FDA NDC Directory · JSON-LD · Markdown

ATROPINE SULFATE

NDC 51662-1626 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA216120
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsATROPINE SULFATE (1 mg/mL)
Marketing started20230713
Package count1

External sources

Source: openFDA. Public-domain (CC0).