lithium carbonate

Generic: lithium carbonate

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium carbonate
Generic Name lithium carbonate
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

lithium carbonate 300 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-763
Product ID 23155-763_09939351-6106-4b21-b923-1b034a6f8f1d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205532
Listing Expiration 2026-12-31
Marketing Start 2020-10-20

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23155763
Hyphenated Format 23155-763

Supplemental Identifiers

RxCUI
197891
UPC
0323155763058 0323155763010
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 ANDA205532 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-01)
  • 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-05)
source: ndc

Packages (2)

23155-763-01 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-01) 23155-763-05 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-05)

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": "09939351-6106-4b21-b923-1b034a6f8f1d", "openfda": {"upc": ["0323155763058", "0323155763010"], "unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["074e3c3b-3a36-4c66-b0a7-e19f9aac8548"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-01)", "package_ndc": "23155-763-01", "marketing_start_date": "20201020"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (23155-763-05)", "package_ndc": "23155-763-05", "marketing_start_date": "20201020"}], "brand_name": "Lithium carbonate", "product_id": "23155-763_09939351-6106-4b21-b923-1b034a6f8f1d", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "23155-763", "generic_name": "Lithium carbonate", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA205532", "marketing_category": "ANDA", "marketing_start_date": "20201020", "listing_expiration_date": "20261231"}