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 CAPSULE, GELATIN COATED
Routes
ORAL
Active Ingredients

lithium carbonate 600 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-172
Product ID 72789-172_40a77777-638f-c92e-e063-6394a90ae6d4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA017812
Listing Expiration 2026-12-31
Marketing Start 1987-01-28

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789172
Hyphenated Format 72789-172

Supplemental Identifiers

RxCUI
197893
UPC
0372789172019
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 NDA017812 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (72789-172-01)
source: ndc

Packages (1)

72789-172-01 100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (72789-172-01)

Ingredients (1)

lithium carbonate (600 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": "40a77777-638f-c92e-e063-6394a90ae6d4", "openfda": {"upc": ["0372789172019"], "unii": ["2BMD2GNA4V"], "rxcui": ["197893"], "spl_set_id": ["16ebe1f9-501d-468b-a37d-f6a46f8f32d1"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (72789-172-01)", "package_ndc": "72789-172-01", "marketing_start_date": "20210312"}], "brand_name": "Lithium Carbonate", "product_id": "72789-172_40a77777-638f-c92e-e063-6394a90ae6d4", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "72789-172", "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": "600 mg/1"}], "application_number": "NDA017812", "marketing_category": "NDA", "marketing_start_date": "19870128", "listing_expiration_date": "20261231"}