lithium carbonate

Generic: lithium carbonate

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

Drug Facts

Product Profile

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

lithium carbonate 150 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3565
Product ID 70518-3565_3c56e37f-02b2-0c0f-e063-6394a90a7b3a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA079139
Listing Expiration 2026-12-31
Marketing Start 2022-10-31

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183565
Hyphenated Format 70518-3565

Supplemental Identifiers

RxCUI
311355
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 ANDA079139 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 150 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BLISTER PACK (70518-3565-0)
  • 100 POUCH in 1 BOX (70518-3565-1) / 1 CAPSULE in 1 POUCH (70518-3565-2)
source: ndc

Packages (2)

Ingredients (1)

lithium carbonate (150 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c56e37f-02b2-0c0f-e063-6394a90a7b3a", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["311355"], "spl_set_id": ["57faf0b0-4380-4bbf-8de7-c3f9d74fc410"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-3565-0)", "package_ndc": "70518-3565-0", "marketing_start_date": "20221031"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-3565-1)  / 1 CAPSULE in 1 POUCH (70518-3565-2)", "package_ndc": "70518-3565-1", "marketing_start_date": "20230928"}], "brand_name": "Lithium Carbonate", "product_id": "70518-3565_3c56e37f-02b2-0c0f-e063-6394a90a7b3a", "dosage_form": "CAPSULE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "70518-3565", "generic_name": "Lithium Carbonate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "150 mg/1"}], "application_number": "ANDA079139", "marketing_category": "ANDA", "marketing_start_date": "20221031", "listing_expiration_date": "20261231"}