FDA NDC Directory · JSON-LD · Markdown

AMINOPHYLLINE

NDC 51662-1341 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA087242
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsAMINOPHYLLINE DIHYDRATE (25 mg/mL)
Marketing started20190210
Package count2

External sources

Source: openFDA. Public-domain (CC0).