FDA NDC Directory · JSON-LD · Markdown

ALBUTEROL SULFATE

NDC 81894-104 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerLuoxin Aurovitas Pharma (Chengdu) Co., Ltd.
Marketing categoryAbbreviated NDA (generic) · App ANDA206224
Dosage form / routeSOLUTION · RESPIRATORY (INHALATION)
Active ingredientsALBUTEROL SULFATE (.83 mg/mL)
Marketing started20171017
Package count4

External sources

Source: openFDA. Public-domain (CC0).