What this pack is
CLEOCIN HCl is the brand name in this record; clindamycin hydrochloride is the generic name. Read both together with the dosage form (oral capsule).
PACK CHECK · MARKET FIRST
The microbiology section of the current U.S. label states that clindamycin binds to the bacterial 50S ribosomal subunit and inhibits protein synthesis. This explains the drug class; symptoms alone cannot identify the cause, susceptibility, whether it should be used or for how long.
Read source: United States ↗Current regulatory record · reviewed 2026-08-28More about its action and precautions →A medicine may use different brand names across markets. Keep the market, brand, generic name, dosage form and route together; one matching field does not prove that two packs are the same or interchangeable.
Use these fields when the pack, market name or package image needs closer checking. They are evidence boundaries, not substitution instructions.
No source-verifiable mainland-China trade-name cue has been established for this record. This does not establish whether the medicine exists, is approved or is available in mainland China. Check pack text and current CDE/NMPA records item by item.
FOR EVERYDAY QUESTIONS
CLEOCIN HCl is the brand name in this record; clindamycin hydrochloride is the generic name. Read both together with the dosage form (oral capsule).
This is a source-traceable public record. It helps you read the product identity and its listed source documents; each market still needs its own current record check.
Bring the actual pack, the label or prescription, and a complete medicine list when you speak with a pharmacist or clinician.
NEXT SAFE STEP
PRODUCT PRESENTATION IDENTITY
Package strength is not an individual dose. These fields help identify the exact labelled product; they do not calculate how much, how often, a missed-use action, splitting, switching or conversion.
How to read a score line: ‘scored’ or ‘unscored’ first identifies this labelled presentation. A score line by itself does not permit self-splitting, reducing or changing the product. Only an explicit statement in the current label for this exact presentation, checked with a pharmacist against the prescription, can support any further handling.
First match the market, dosage form and labelled amount on the pack in hand. The number of tablets, sachets or devices in a pack is not a personal dose or schedule.
United States label · Current U.S. DailyMed public label (updated 8 Apr 2026; published 9 Apr 2026, SPL v40)
United States label · Current U.S. DailyMed public label (updated 8 Apr 2026; published 9 Apr 2026, SPL v40)
United States label · Current U.S. DailyMed public label (updated 8 Apr 2026; published 9 Apr 2026, SPL v40)
PUBLIC LABEL IMAGE
This current public-label package panel helps check the brand, generic name, strength and dosage-form clues only. It does not authenticate a product in hand or establish originator status, availability, sale eligibility, another package or another market.
Open the public label source ↗LABEL READING · NOT A PRESCRIPTION
Reading level: drug-specific label reading. This record has been expanded around its dosage form or a higher-risk reading question; the current target-market label and professional review still apply.
The current U.S. label has a boxed warning and separately lists 75, 150 and 300 mg oral capsules. This module helps ordinary readers identify the exact product, recognise symptoms requiring prompt help and return individual questions to the prescription and professional review; it gives no personal capsule count, interval or course.
PHARMACOVIGILANCE · OFFICIAL ROUTES
Start with the public label or product record linked to this dossier, then use the official safety routes below for the market that applies to the medicine in hand.
This checklist only helps organise the right question. It does not create a personal conclusion about stopping, switching, dose, combination or suitability.
This dossier’s publicly accessible product-level route has been checked individually. It does not mean that real-time alerts in every country or region have been searched, or that the medicine has or does not have a current risk.
This is a document-coverage summary, not a claim that the medicine is authorised, supplied, interchangeable or actively monitored in every listed market today.
This is not a conclusion that the medicine has no risk, warning, recall or newer notice in another market. Start with the checked product-level label above, then use the official market gateways below for the product in hand.
See the reviewed safety-record directory →This card brings together the medicine-specific product route and 15 market-level official vigilance gateways. It does not mean real-time alerts for this medicine have been searched in every country or region, or that the medicine has a new alert, recall or risk conclusion. Match brand, generic name, dosage form, strength, market and notice date item by item; do not self-stop, switch, increase or reduce use from a headline.
For severe or rapidly worsening symptoms, suspected overdose, a severe allergic reaction, loss of consciousness or another emergency, use local emergency services. Do not wait for an online alert search or change a medicine from this page.
PRIVATE FAMILY LIST
Only the brand, generic name, dosage form and route are added, and they stay in this browser. Copy strength, label directions, start/stop history and any concern from the actual pack; this tool does not calculate a dose or decide combination, switching or stopping.
Add to the family medicine list →PACK · LABEL · MEDICINE LIST
Use this card to organise questions about CLEOCIN HCl (clindamycin hydrochloride). Keep the exact pack, its current label and the full medicine list together.
CLEOCIN HCl is the brand in this record and clindamycin hydrochloride is the active-ingredient name. Check both with the dosage form (Dosage form and presentation as documented in the linked primary label) and the market on the actual pack.
mg, mcg, mg/mL or a percentage describes the labelled amount in one tablet, capsule, measured volume, spray or other unit. It is not an answer to how many units a person should take.
Before splitting, crushing, chewing or opening anything, find an explicit instruction for this exact product in its current label and ask a pharmacist. A score line or a previous pack is not enough by itself.
Include prescriptions, over-the-counter products, eye drops, creams, vitamins, minerals, herbs and supplements. A pharmacist or prescriber needs the whole list before any combination, alternation, switch or stop is considered.
Ask which medicine, which gene and what clinical decision a result could change. A gene–drug association does not mean broad genetic testing is needed for everyone and must not be used to change treatment without professional review.
For a suspected overdose, a severe allergic reaction, fainting or difficulty breathing, use the local emergency or poison-information service now. Do not wait for a website reply or alter several medicines to test what caused it.
This card does not calculate a dose, decide whether medicines can be combined, or replace a clinician or pharmacist. Market-specific current labels and the person's full context still need review.
HOW IT WORKS · NOT A TREATMENT PLAN
SOURCE EVIDENCE REGISTER
Every public link is labelled with its market, document status and document type. A historical public record is not a current label, and an official lookup entry is not a product-specific record.
SOURCE-TRACEABLE ARCHIVE
This page includes an exact current U.S. public-label package panel for CLEOCIN HCl, alongside documentary primary-source material. It helps check product identity, but does not itself establish originator status, product quality, availability or sale eligibility.
DOCUMENT TIMELINE
All three capsule product tables in the current label list NDA 050162 and a marketing start date of 22 May 1970. This node locates this U.S. oral-capsule record only; it does not establish approval, supply, originator/generic relationship or individual suitability in another market.
DailyMed (NLM): current U.S. CLEOCIN HCl clindamycin-hydrochloride oral-capsule label (Pharmacia & Upjohn; SPL v40) ↗DailyMed lists the current label as updated 8 Apr 2026 and SPL v40 as published 9 Apr 2026. The date identifies the document version; it is not anyone's start date, frequency, course or a stock finding.
DailyMed (NLM): current U.S. CLEOCIN HCl clindamycin-hydrochloride oral-capsule label (Pharmacia & Upjohn; SPL v40) ↗MARKET SCOPE
The dossier separately records the NDC, colour, imprint and 100-capsule bottle panel for 75, 150 and 300 mg capsules. A label page does not establish local stock, purchase availability, individual suitability or self-switching between strengths.
No local trade name, approval, packaging, supply, sale eligibility, originator/generic relationship or interchangeability is inferred from the U.S. label, brand, NDA, package panel or shared generic name.
Read each document in its stated market, date and dosage-form context. A historical record is not a current label and does not support individual medical, substitution or purchasing conclusions.
This page has a U.S. public history/regulatory archive but no mainland China record for this specific product. That does not establish whether the medicine exists, is approved or is available in mainland China. Verify product identity, dosage form, strength, holder and the current label item by item.
RECORD FAQ
No. 150 mg is only the labelled clindamycin-equivalent amount in this exact capsule. Individual capsule count, frequency, course and suitability must come from the exact prescription and professional review of the infection, allergy history, organ function and complete medicine list.
Do not do this yourself. The current label defines CLEOCIN HCl as an oral capsule and emphasises a full glass of water and time before lying down. The page has no evidence to present opening, visually halving or mixing the capsule as a safe alternative. Ask a pharmacist or prescriber to check an exact suitable form and plan before changing it.
READ NEXT
The listed links are public sources selected for traceability. They must be rechecked against the current target-market record before any use beyond reading and research.