lithium carbonate

Generic: lithium carbonate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium carbonate
Generic Name lithium carbonate
Labeler bryant ranch prepack
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

lithium carbonate 300 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 63629-1917
Product ID 63629-1917_6391a7eb-907d-418b-aa66-b39dc038f60e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090702
Listing Expiration 2026-12-31
Marketing Start 2009-12-15

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 636291917
Hyphenated Format 63629-1917

Supplemental Identifiers

RxCUI
197889
UNII
2BMD2GNA4V

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 ANDA090702 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 1000 CAPSULE in 1 BOTTLE (63629-1917-1)
source: ndc

Packages (1)

63629-1917-1 1000 CAPSULE in 1 BOTTLE (63629-1917-1)

Ingredients (1)

lithium carbonate (300 mg/1)

Linked Drug Pages (1)

lithium carbonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6391a7eb-907d-418b-aa66-b39dc038f60e", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197889"], "spl_set_id": ["cc6f07db-c9e6-4e2d-90f8-00868954594d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (63629-1917-1)", "package_ndc": "63629-1917-1", "marketing_start_date": "20091215"}], "brand_name": "lithium carbonate", "product_id": "63629-1917_6391a7eb-907d-418b-aa66-b39dc038f60e", "dosage_form": "CAPSULE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "63629-1917", "generic_name": "lithium carbonate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "lithium carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA090702", "marketing_category": "ANDA", "marketing_start_date": "20091215", "listing_expiration_date": "20261231"}