Active Ingredient: ALBUTEROL SULFATE
Proprietary Name: ALBUTEROL SULFATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 2MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A072817
Product Number: 001
Approval Date: Jan 9, 1990
Applicant Holder Full Name: WARNER CHILCOTT DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information