Product Details for ANDA 040897
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: A040897
Product Number: 001
Approval Date: Apr 22, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES 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: A040897
Product Number: 001
Approval Date: Apr 22, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES 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: A040897
Product Number: 002
Approval Date: Apr 22, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES 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: A040897
Product Number: 002
Approval Date: Apr 22, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES 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: A040897
Product Number: 003
Approval Date: Apr 22, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES 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: A040897
Product Number: 003
Approval Date: Apr 22, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES 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: A040897
Product Number: 004
Approval Date: Apr 22, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES 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: A040897
Product Number: 004
Approval Date: Apr 22, 2009
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information