lithium carbonate

Generic: lithium carbonate

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium carbonate
Generic Name lithium carbonate
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lithium carbonate 300 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 62756-430
Product ID 62756-430_b0888aa2-be9d-4a45-81b2-a59493bc4892
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091027
Listing Expiration 2026-12-31
Marketing Start 2010-07-08

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62756430
Hyphenated Format 62756-430

Supplemental Identifiers

RxCUI
197890
UPC
0362756430884
UNII
2BMD2GNA4V

Packaging Origin

Original Packager
true

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 ANDA091027 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (62756-430-08)
  • 1000 TABLET in 1 BOTTLE (62756-430-18)
  • 30 TABLET in 1 BOTTLE (62756-430-83)
  • 100 TABLET in 1 BOTTLE (62756-430-88)
source: ndc

Packages (4)

62756-430-08 100 TABLET in 1 BOTTLE (62756-430-08) 62756-430-18 1000 TABLET in 1 BOTTLE (62756-430-18) 62756-430-83 30 TABLET in 1 BOTTLE (62756-430-83) 62756-430-88 100 TABLET in 1 BOTTLE (62756-430-88)

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": "b0888aa2-be9d-4a45-81b2-a59493bc4892", "openfda": {"upc": ["0362756430884"], "unii": ["2BMD2GNA4V"], "rxcui": ["197890"], "spl_set_id": ["d3284649-ed4c-4096-987b-4ac16b8278f2"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62756-430-08)", "package_ndc": "62756-430-08", "marketing_start_date": "20100708"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (62756-430-18)", "package_ndc": "62756-430-18", "marketing_start_date": "20100708"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (62756-430-83)", "package_ndc": "62756-430-83", "marketing_start_date": "20100708"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (62756-430-88)", "package_ndc": "62756-430-88", "marketing_start_date": "20100708"}], "brand_name": "Lithium Carbonate", "product_id": "62756-430_b0888aa2-be9d-4a45-81b2-a59493bc4892", "dosage_form": "TABLET", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "62756-430", "generic_name": "Lithium Carbonate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA091027", "marketing_category": "ANDA", "marketing_start_date": "20100708", "listing_expiration_date": "20261231"}