lithium carbonate

Generic: lithium carbonate

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium carbonate
Generic Name lithium carbonate
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

lithium carbonate 300 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-174
Product ID 72789-174_2becc6b3-fa7f-6bdc-e063-6394a90a8098
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018558
Listing Expiration 2026-12-31
Marketing Start 1982-01-29

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789174
Hyphenated Format 72789-174

Supplemental Identifiers

RxCUI
197890
UPC
0372789174013
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
  • 100 TABLET in 1 BOTTLE, PLASTIC (72789-174-01)
source: ndc

Packages (1)

72789-174-01 100 TABLET in 1 BOTTLE, PLASTIC (72789-174-01)

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": "2becc6b3-fa7f-6bdc-e063-6394a90a8098", "openfda": {"upc": ["0372789174013"], "unii": ["2BMD2GNA4V"], "rxcui": ["197890"], "spl_set_id": ["d20ed2aa-aa56-4709-9e7a-9243c71465c9"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72789-174-01)", "package_ndc": "72789-174-01", "marketing_start_date": "20210309"}], "brand_name": "Lithium Carbonate", "product_id": "72789-174_2becc6b3-fa7f-6bdc-e063-6394a90a8098", "dosage_form": "TABLET", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "72789-174", "generic_name": "Lithium Carbonate", "labeler_name": "PD-Rx Pharmaceuticals, 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": "19820129", "listing_expiration_date": "20261231"}