Package 23155-763-05

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 23155-763-05
Digits Only 2315576305
Product NDC 23155-763
Product ID 23155-763_09939351-6106-4b21-b923-1b034a6f8f1d
Description

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-05)

Marketing

Marketing Status
Marketed Since 2020-10-20
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": "09939351-6106-4b21-b923-1b034a6f8f1d", "openfda": {"upc": ["0323155763058", "0323155763010"], "unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["074e3c3b-3a36-4c66-b0a7-e19f9aac8548"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-01)", "package_ndc": "23155-763-01", "marketing_start_date": "20201020"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-05)", "package_ndc": "23155-763-05", "marketing_start_date": "20201020"}], "brand_name": "Lithium carbonate", "product_id": "23155-763_09939351-6106-4b21-b923-1b034a6f8f1d", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "23155-763", "generic_name": "Lithium carbonate", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA205532", "marketing_category": "ANDA", "marketing_start_date": "20201020", "listing_expiration_date": "20261231"}