Product Details for ANDA 040721
BETHANECHOL CHLORIDE (BETHANECHOL CHLORIDE)
5MG
Marketing Status: Discontinued
10MG
Marketing Status: Discontinued
25MG
Marketing Status: Discontinued
50MG
Marketing Status: Discontinued
5MG
Marketing Status: Discontinued
Active Ingredient: BETHANECHOL CHLORIDE
Proprietary Name: BETHANECHOL CHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040721
Product Number: 001
Approval Date: Nov 1, 2006
Applicant Holder Full Name: IMPAX LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
BETHANECHOL CHLORIDE (BETHANECHOL CHLORIDE)
Proprietary Name: BETHANECHOL CHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040721
Product Number: 001
Approval Date: Nov 1, 2006
Applicant Holder Full Name: IMPAX LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
10MG
Marketing Status: Discontinued
Active Ingredient: BETHANECHOL CHLORIDE
Proprietary Name: BETHANECHOL CHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040721
Product Number: 002
Approval Date: Nov 1, 2006
Applicant Holder Full Name: IMPAX LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
BETHANECHOL CHLORIDE (BETHANECHOL CHLORIDE)
Proprietary Name: BETHANECHOL CHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040721
Product Number: 002
Approval Date: Nov 1, 2006
Applicant Holder Full Name: IMPAX LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
25MG
Marketing Status: Discontinued
Active Ingredient: BETHANECHOL CHLORIDE
Proprietary Name: BETHANECHOL CHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040721
Product Number: 003
Approval Date: Nov 1, 2006
Applicant Holder Full Name: IMPAX LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
BETHANECHOL CHLORIDE (BETHANECHOL CHLORIDE)
Proprietary Name: BETHANECHOL CHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040721
Product Number: 003
Approval Date: Nov 1, 2006
Applicant Holder Full Name: IMPAX LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
50MG
Marketing Status: Discontinued
Active Ingredient: BETHANECHOL CHLORIDE
Proprietary Name: BETHANECHOL CHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040721
Product Number: 004
Approval Date: Nov 1, 2006
Applicant Holder Full Name: IMPAX LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: BETHANECHOL CHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040721
Product Number: 004
Approval Date: Nov 1, 2006
Applicant Holder Full Name: IMPAX LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information