lithium carbonate

Generic: lithium carbonate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium carbonate
Generic Name lithium carbonate
Labeler remedyrepack inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lithium carbonate 300 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-1481
Product ID 70518-1481_4910b637-1083-f6b5-e063-6294a90adb25
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018558
Listing Expiration 2027-12-31
Marketing Start 2018-10-06

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705181481
Hyphenated Format 70518-1481

Supplemental Identifiers

RxCUI
197890
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 NDA018558 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BLISTER PACK (70518-1481-1)
source: ndc

Packages (1)

70518-1481-1 30 TABLET in 1 BLISTER PACK (70518-1481-1)

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": "4910b637-1083-f6b5-e063-6294a90adb25", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197890"], "spl_set_id": ["c84cce95-cfcb-4426-aac6-d2f48f946ada"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1481-1)", "package_ndc": "70518-1481-1", "marketing_start_date": "20230608"}], "brand_name": "Lithium Carbonate", "product_id": "70518-1481_4910b637-1083-f6b5-e063-6294a90adb25", "dosage_form": "TABLET", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "70518-1481", "generic_name": "Lithium Carbonate", "labeler_name": "REMEDYREPACK 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": "20181006", "listing_expiration_date": "20271231"}