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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
LANOXIN Injection
Generic name / active ingredient
digoxin injection
Dosage-form class
Digoxin injection: 500 mcg/2 mL (250 mcg/mL) single-dose vial; LANOXIN Injection Pediatric 100 mcg/mL single-dose vial (as listed in the current U.S. label)
Route
Intramuscular / intravenous injection
Record reviewed
2026-08-21

Copy from the pack in hand

Source-linked reading points

  • The adult vial is 500 mcg/2 mL (250 mcg/mL); the Pediatric vial is 100 mcg/mL and 1 mL. They are different label identities; this page does not turn concentration, vial total or mL into an individual injection amount or converter.
  • Continue by checking the NDC: the adult single-dose vial is 70515-261-10 and the Pediatric single-dose vial is 70515-263-10. A shared brand, generic name or the word “injection” is not enough to exchange the two vials.
  • The current label also lists adult and pediatric ampules with a stated marketing-end date. This page does not present them as current packages or infer any real-world supply or availability.
  • LANOXIN tablets, generic digoxin oral solution and this injection belong to different form, NDA or label chains. Do not self-convert, substitute, combine or change use by mcg, mL, route or brand name.

Reviewed presentation examples — compare every field

  • 500 mcg/2 mL (250 mcg/mL); 10 single-dose vialsNDC 70515-261-10
  • 100 mcg/mL; 1 mL; 10 single-dose vialsNDC 70515-263-10

EDITORIAL RECORD

Who prepared and checked this page

Byline
OriginDrug Content Editorial
Review role
Public primary-source verification
Last reviewed
2026-08-21
Source record
1 clickable primary-source entry point is 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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