Package 67046-1575-3

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 67046-1575-3
Digits Only 6704615753
Product NDC 67046-1575
Product ID 67046-1575_3dfedfb7-e561-bc6d-e063-6294a90ac562
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (67046-1575-3)

Marketing

Marketing Status
Marketed Since 2025-09-04
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": "3dfedfb7-e561-bc6d-e063-6294a90ac562", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["3dfeeb11-a096-ae17-e063-6294a90a9aae"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (67046-1575-3)", "package_ndc": "67046-1575-3", "marketing_start_date": "20250904"}], "brand_name": "Lithium Carbonate", "product_id": "67046-1575_3dfedfb7-e561-bc6d-e063-6294a90ac562", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "67046-1575", "generic_name": "Lithium Carbonate", "labeler_name": "Coupler LLC", "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": "20250904", "listing_expiration_date": "20261231"}