lithium carbonate

Generic: lithium carbonate

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

Drug Facts

Product Profile

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

lithium carbonate 300 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-171
Product ID 72789-171_419df69c-92e0-79f5-e063-6294a90a3e68
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076832
Listing Expiration 2026-12-31
Marketing Start 2004-10-28

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789171
Hyphenated Format 72789-171

Supplemental Identifiers

RxCUI
197891
UPC
0372789171821
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 ANDA076832 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-171-82)
source: ndc

Packages (1)

72789-171-82 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-171-82)

Ingredients (1)

lithium carbonate (300 mg/1)

Linked Drug Pages (2)

Lithium Carbonate ndc-match (0.9) Lithium Carbonate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "419df69c-92e0-79f5-e063-6294a90a3e68", "openfda": {"upc": ["0372789171821"], "unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["039f188c-413a-6e64-e063-6294a90a2972"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-171-82)", "package_ndc": "72789-171-82", "marketing_start_date": "20230823"}], "brand_name": "Lithium Carbonate", "product_id": "72789-171_419df69c-92e0-79f5-e063-6294a90a3e68", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "72789-171", "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": "ANDA076832", "marketing_category": "ANDA", "marketing_start_date": "20041028", "listing_expiration_date": "20261231"}