lithium carbonate

Generic: lithium carbonate

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

Drug Facts

Product Profile

Brand Name lithium carbonate
Generic Name lithium carbonate
Labeler alembic pharmaceuticals inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

lithium carbonate 300 mg/1

Manufacturer
Alembic Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 62332-148
Product ID 62332-148_ef84d260-7533-4539-a765-71f39412c34a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204445
Listing Expiration 2026-12-31
Marketing Start 2017-02-21

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62332148
Hyphenated Format 62332-148

Supplemental Identifiers

RxCUI
197891
UPC
0362332148301
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 ANDA204445 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 80 TABLET, EXTENDED RELEASE in 1 CARTON (62332-148-08)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-30)
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-31)
  • 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-91)
source: ndc

Packages (4)

62332-148-08 80 TABLET, EXTENDED RELEASE in 1 CARTON (62332-148-08) 62332-148-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-30) 62332-148-31 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-31) 62332-148-91 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-91)

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": "ef84d260-7533-4539-a765-71f39412c34a", "openfda": {"upc": ["0362332148301"], "unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["a1e2f942-2bc0-4afd-91ad-6c4cab38c8f0"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "80 TABLET, EXTENDED RELEASE in 1 CARTON (62332-148-08)", "package_ndc": "62332-148-08", "marketing_start_date": "20170221"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-30)", "package_ndc": "62332-148-30", "marketing_start_date": "20170221"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-31)", "package_ndc": "62332-148-31", "marketing_start_date": "20170221"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-148-91)", "package_ndc": "62332-148-91", "marketing_start_date": "20170221"}], "brand_name": "Lithium Carbonate", "product_id": "62332-148_ef84d260-7533-4539-a765-71f39412c34a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "62332-148", "generic_name": "Lithium Carbonate", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA204445", "marketing_category": "ANDA", "marketing_start_date": "20170221", "listing_expiration_date": "20261231"}