Active Ingredient: ALBUTEROL SULFATE
Proprietary Name: ALBUTEROL SULFATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 4MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A072780
Product Number: 001
Approval Date: Jun 25, 1993
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information