Package 72789-174-01

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 72789-174-01
Digits Only 7278917401
Product NDC 72789-174
Product ID 72789-174_2becc6b3-fa7f-6bdc-e063-6394a90a8098
Description

100 TABLET in 1 BOTTLE, PLASTIC (72789-174-01)

Marketing

Marketing Status
Marketed Since 2021-03-09
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": "2becc6b3-fa7f-6bdc-e063-6394a90a8098", "openfda": {"upc": ["0372789174013"], "unii": ["2BMD2GNA4V"], "rxcui": ["197890"], "spl_set_id": ["d20ed2aa-aa56-4709-9e7a-9243c71465c9"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-174-01)", "package_ndc": "72789-174-01", "marketing_start_date": "20210309"}], "brand_name": "Lithium Carbonate", "product_id": "72789-174_2becc6b3-fa7f-6bdc-e063-6394a90a8098", "dosage_form": "TABLET", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "72789-174", "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": "NDA018558", "marketing_category": "NDA", "marketing_start_date": "19820129", "listing_expiration_date": "20261231"}