Package 72789-171-82

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 72789-171-82
Digits Only 7278917182
Product NDC 72789-171
Product ID 72789-171_419df69c-92e0-79f5-e063-6294a90a3e68
Description

500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-171-82)

Marketing

Marketing Status
Marketed Since 2023-08-23
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": "419df69c-92e0-79f5-e063-6294a90a3e68", "openfda": {"upc": ["0372789171821"], "unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["039f188c-413a-6e64-e063-6294a90a2972"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-171-82)", "package_ndc": "72789-171-82", "marketing_start_date": "20230823"}], "brand_name": "Lithium Carbonate", "product_id": "72789-171_419df69c-92e0-79f5-e063-6294a90a3e68", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "72789-171", "generic_name": "Lithium Carbonate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA076832", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}