FDA NDC Directory · JSON-LD · Markdown

Atropine Sulfate

NDC 70069-631 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215969
Dosage form / routeSOLUTION · INTRAVENOUS
Active ingredientsATROPINE SULFATE (.4 mg/mL)
Marketing started20240704
Package count1

External sources

Source: openFDA. Public-domain (CC0).