lithium carbonate
Generic: lithium carbonate
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
lithium carbonate
Generic Name
lithium carbonate
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
lithium carbonate 450 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0054-0020
Product ID
0054-0020_17dfc90a-8988-4e63-aaa0-9c88c4a7d1bf
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076691
Listing Expiration
2026-12-31
Marketing Start
2004-01-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00540020
Hyphenated Format
0054-0020
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
lithium carbonate (source: ndc)
Generic Name
lithium carbonate (source: ndc)
Application Number
ANDA076691 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 450 mg/1
Packaging
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0054-0020-25)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
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"}