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PACK IN HAND · ONE-PAGE CHECK

Medicine pack check sheet

Print this sheet or fill it in before speaking with a pharmacist or clinician. Copy only what is printed on the pack in hand. The published fields below are starting points from this record, not proof that your pack is the same product.

Published record starting point

Record display name
Procardia XL
Generic name / active ingredient
nifedipine
Dosage-form class
Controlled-release oral tablets(GITS; 30, 60, 90 mg; as listed in the 2025 DailyMed label)
Route
Oral
Record reviewed
2026-08-20

Copy from the pack in hand

Source-linked reading points

  • 30, 60 and 90 mg are labelled strengths for controlled-release tablets, not rules for adding, halving or converting tablet counts by experience with another nifedipine product. Any product change requires the exact prescription, dosage form, market and current label to be checked together.
  • The DailyMed label explicitly states that the controlled-release tablet should be swallowed whole, not chewed, divided or crushed. This ‘do not split’ statement comes from the release design of this exact product and cannot be generalised to another tablet.
  • The label explains that, after release is complete, something that looks like a tablet shell may occasionally be seen in stool. That is not a reason to self-dose again, stop or change the plan; bring any concern, the actual package and the complete medicine list to a pharmacist or prescribing team.
  • Related blood-pressure medicines, beta blockers, other cardiovascular medicines, grapefruit products or multiple medicines can all raise questions needing professional review. Do not self-combine, alternate or substitute merely because packages mention blood pressure or contain nifedipine; seek timely local medical support for dizziness, chest discomfort, fainting or marked illness.

Reviewed presentation examples — compare every field

  • 30 mg labelled strength; 33 mg tablet content; 100-tablet bottle (GITS controlled-release tablet)NDC 0069-2650-66
  • 60 mg labelled strength; 66 mg tablet content; 100-tablet bottle (GITS controlled-release tablet)NDC 0069-2660-66
  • 90 mg labelled strength; 99 mg tablet content; 100-tablet bottle (GITS controlled-release tablet)NDC 0069-2670-66

EDITORIAL RECORD

Who prepared and checked this page

Byline
OriginDrug Content Editorial
Review role
Public primary-source verification
Last reviewed
2026-08-20
Source record
3 clickable primary-source entry points are listed with this dossier.

The review role checks source traceability, stated market, document version and product-identity fields. It is not a claim of clinical licensure, prescribing authority or individual pharmacy service. Read the editorial policy.

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