Product Details for ANDA 085447
A-POXIDE (CHLORDIAZEPOXIDE HYDROCHLORIDE)
5MG
Marketing Status: Discontinued
10MG
Marketing Status: Discontinued
25MG
Marketing Status: Discontinued
5MG
Marketing Status: Discontinued
Active Ingredient: CHLORDIAZEPOXIDE HYDROCHLORIDE
Proprietary Name: A-POXIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A085447
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
A-POXIDE (CHLORDIAZEPOXIDE HYDROCHLORIDE)
Proprietary Name: A-POXIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A085447
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
10MG
Marketing Status: Discontinued
Active Ingredient: CHLORDIAZEPOXIDE HYDROCHLORIDE
Proprietary Name: A-POXIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A085447
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
A-POXIDE (CHLORDIAZEPOXIDE HYDROCHLORIDE)
Proprietary Name: A-POXIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A085447
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
25MG
Marketing Status: Discontinued
Active Ingredient: CHLORDIAZEPOXIDE HYDROCHLORIDE
Proprietary Name: A-POXIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A085447
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: A-POXIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A085447
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information