Product Details for ANDA 040893
MEPERIDINE HYDROCHLORIDE (MEPERIDINE HYDROCHLORIDE)
50MG
Marketing Status: Prescription
75MG
Marketing Status: Discontinued
100MG
Marketing Status: Discontinued
150MG
Marketing Status: Discontinued
50MG
Marketing Status: Prescription
Active Ingredient: MEPERIDINE HYDROCHLORIDE
Proprietary Name: MEPERIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A040893
Product Number: 001
Approval Date: Jun 24, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Prescription
Patent and Exclusivity Information
MEPERIDINE HYDROCHLORIDE (MEPERIDINE HYDROCHLORIDE)
Proprietary Name: MEPERIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A040893
Product Number: 001
Approval Date: Jun 24, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Prescription
Patent and Exclusivity Information
75MG
Marketing Status: Discontinued
Active Ingredient: MEPERIDINE HYDROCHLORIDE
Proprietary Name: MEPERIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 75MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040893
Product Number: 002
Approval Date: Jun 24, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
MEPERIDINE HYDROCHLORIDE (MEPERIDINE HYDROCHLORIDE)
Proprietary Name: MEPERIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 75MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040893
Product Number: 002
Approval Date: Jun 24, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
100MG
Marketing Status: Discontinued
Active Ingredient: MEPERIDINE HYDROCHLORIDE
Proprietary Name: MEPERIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040893
Product Number: 003
Approval Date: Jun 24, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
MEPERIDINE HYDROCHLORIDE (MEPERIDINE HYDROCHLORIDE)
Proprietary Name: MEPERIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040893
Product Number: 003
Approval Date: Jun 24, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
150MG
Marketing Status: Discontinued
Active Ingredient: MEPERIDINE HYDROCHLORIDE
Proprietary Name: MEPERIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040893
Product Number: 004
Approval Date: Jun 24, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: MEPERIDINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A040893
Product Number: 004
Approval Date: Jun 24, 2009
Applicant Holder Full Name: GENUS LIFESCIENCES INC
Marketing Status: Discontinued
Patent and Exclusivity Information