Package 68462-223-01

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 68462-223-01
Digits Only 6846222301
Product NDC 68462-223
Product ID 68462-223_851bb451-d546-4bc8-9c37-90b91c7ea5c5
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-223-01)

Marketing

Marketing Status
Marketed Since 2010-12-27
Brand lithium carbonate
Generic lithium carbonate
Sample Package No

Linked Drug Pages (1)

Lithium Carbonate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "851bb451-d546-4bc8-9c37-90b91c7ea5c5", "openfda": {"upc": ["0368462223017"], "unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["1b65d27e-5086-4a87-8387-c49f3d060978"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-223-01)", "package_ndc": "68462-223-01", "marketing_start_date": "20101227"}], "brand_name": "Lithium Carbonate", "product_id": "68462-223_851bb451-d546-4bc8-9c37-90b91c7ea5c5", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "68462-223", "generic_name": "Lithium Carbonate", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA091544", "marketing_category": "ANDA", "marketing_start_date": "20101227", "listing_expiration_date": "20271231"}