Package 0054-0020-25

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 0054-0020-25
Digits Only 0054002025
Product NDC 0054-0020
Product ID 0054-0020_17dfc90a-8988-4e63-aaa0-9c88c4a7d1bf
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0020-25)

Marketing

Marketing Status
Marketed Since 2004-01-13
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": "17dfc90a-8988-4e63-aaa0-9c88c4a7d1bf", "openfda": {"upc": ["0300540020255"], "unii": ["2BMD2GNA4V"], "rxcui": ["197892"], "spl_set_id": ["a226a88d-eb57-4c96-afda-939801bca0a9"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0020-25)", "package_ndc": "0054-0020-25", "marketing_start_date": "20040113"}], "brand_name": "Lithium Carbonate", "product_id": "0054-0020_17dfc90a-8988-4e63-aaa0-9c88c4a7d1bf", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "0054-0020", "generic_name": "Lithium Carbonate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "450 mg/1"}], "application_number": "ANDA076691", "marketing_category": "ANDA", "marketing_start_date": "20040113", "listing_expiration_date": "20261231"}