Package 72789-172-01

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 72789-172-01
Digits Only 7278917201
Product NDC 72789-172
Product ID 72789-172_40a77777-638f-c92e-e063-6394a90ae6d4
Description

100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (72789-172-01)

Marketing

Marketing Status
Marketed Since 2021-03-12
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": "40a77777-638f-c92e-e063-6394a90ae6d4", "openfda": {"upc": ["0372789172019"], "unii": ["2BMD2GNA4V"], "rxcui": ["197893"], "spl_set_id": ["16ebe1f9-501d-468b-a37d-f6a46f8f32d1"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (72789-172-01)", "package_ndc": "72789-172-01", "marketing_start_date": "20210312"}], "brand_name": "Lithium Carbonate", "product_id": "72789-172_40a77777-638f-c92e-e063-6394a90ae6d4", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "72789-172", "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": "600 mg/1"}], "application_number": "NDA017812", "marketing_category": "NDA", "marketing_start_date": "19870128", "listing_expiration_date": "20261231"}