FDA NDC Directory · JSON-LD · Markdown

ALBUTEROL SULFATE

NDC 81894-106 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerLuoxin Aurovitas Pharma (Chengdu) Co., Ltd.
Marketing categoryAbbreviated NDA (generic) · App ANDA211888
Dosage form / routeSOLUTION · RESPIRATORY (INHALATION)
Active ingredientsALBUTEROL SULFATE (1.25 mg/3mL)
Marketing started20200420
Package count2

External sources

Source: openFDA. Public-domain (CC0).