Product Details for ANDA 076823
LITHIUM CARBONATE (LITHIUM CARBONATE)
150MG
Marketing Status: Discontinued
300MG
Marketing Status: Discontinued
600MG
Marketing Status: Discontinued
150MG
Marketing Status: Discontinued
Active Ingredient: LITHIUM CARBONATE
Proprietary Name: LITHIUM CARBONATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076823
Product Number: 001
Approval Date: Jun 29, 2004
Applicant Holder Full Name: ABLE LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
LITHIUM CARBONATE (LITHIUM CARBONATE)
Proprietary Name: LITHIUM CARBONATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076823
Product Number: 001
Approval Date: Jun 29, 2004
Applicant Holder Full Name: ABLE LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
300MG
Marketing Status: Discontinued
Active Ingredient: LITHIUM CARBONATE
Proprietary Name: LITHIUM CARBONATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076823
Product Number: 002
Approval Date: Jun 29, 2004
Applicant Holder Full Name: ABLE LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
LITHIUM CARBONATE (LITHIUM CARBONATE)
Proprietary Name: LITHIUM CARBONATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076823
Product Number: 002
Approval Date: Jun 29, 2004
Applicant Holder Full Name: ABLE LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
600MG
Marketing Status: Discontinued
Active Ingredient: LITHIUM CARBONATE
Proprietary Name: LITHIUM CARBONATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076823
Product Number: 003
Approval Date: Jun 29, 2004
Applicant Holder Full Name: ABLE LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: LITHIUM CARBONATE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A076823
Product Number: 003
Approval Date: Jun 29, 2004
Applicant Holder Full Name: ABLE LABORATORIES INC
Marketing Status: Discontinued
Patent and Exclusivity Information