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
Routes
Active Ingredients
lithium carbonate 300 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0054-8528
Product ID
0054-8528_a9e58e66-6569-4c3b-993f-b4236904296e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018558
Listing Expiration
2026-12-31
Marketing Start
1982-06-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00548528
Hyphenated Format
0054-8528
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
NDA018558 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
Packaging
- 10 TABLET in 1 BLISTER PACK (0054-8528-25)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a9e58e66-6569-4c3b-993f-b4236904296e", "openfda": {"upc": ["0300543527638"], "unii": ["2BMD2GNA4V"], "rxcui": ["197889", "197890", "197893", "311355", "756059"], "spl_set_id": ["7dc9c6d2-6d9a-49e4-a8ab-437b0ed5f84e"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET in 1 BLISTER PACK (0054-8528-25)", "package_ndc": "0054-8528-25", "marketing_start_date": "19820614"}], "brand_name": "Lithium Carbonate", "product_id": "0054-8528_a9e58e66-6569-4c3b-993f-b4236904296e", "dosage_form": "TABLET", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "0054-8528", "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": "NDA018558", "marketing_category": "NDA", "marketing_start_date": "19820614", "listing_expiration_date": "20261231"}