Package 0054-0021-29

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 0054-0021-29
Digits Only 0054002129
Product NDC 0054-0021
Description

500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0021-29)

Marketing

Marketing Status
Marketed Since 2004-10-28
Brand lithium carbonate
Generic lithium carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5e0351f3-360d-4044-a40a-a36f0008cf92", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["c612b6c5-eeb9-4fdd-8c85-bb3d2147cd1e"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0021-25)", "package_ndc": "0054-0021-25", "marketing_start_date": "20041028"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0021-29)", "package_ndc": "0054-0021-29", "marketing_start_date": "20041028"}], "brand_name": "Lithium Carbonate", "product_id": "0054-0021_5e0351f3-360d-4044-a40a-a36f0008cf92", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "0054-0021", "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": "300 mg/1"}], "application_number": "ANDA076832", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}