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 450 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-901
Product ID 43063-901_415d2a6b-7242-213c-e063-6294a90a5092
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076691
Listing Expiration 2026-12-31
Marketing Start 2004-01-13

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063901
Hyphenated Format 43063-901

Supplemental Identifiers

RxCUI
197892
UPC
0343063901014
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 ANDA076691 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 450 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-901-01)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-901-30)
source: ndc

Packages (2)

43063-901-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-901-01) 43063-901-30 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-901-30)

Ingredients (1)

lithium carbonate (450 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": "415d2a6b-7242-213c-e063-6294a90a5092", "openfda": {"upc": ["0343063901014"], "unii": ["2BMD2GNA4V"], "rxcui": ["197892"], "spl_set_id": ["edfceebd-a3e4-4905-bffe-cdc0b948dcd2"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-901-01)", "package_ndc": "43063-901-01", "marketing_start_date": "20180925"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-901-30)", "package_ndc": "43063-901-30", "marketing_start_date": "20230728"}], "brand_name": "Lithium Carbonate", "product_id": "43063-901_415d2a6b-7242-213c-e063-6294a90a5092", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "43063-901", "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": "450 mg/1"}], "application_number": "ANDA076691", "marketing_category": "ANDA", "marketing_start_date": "20040113", "listing_expiration_date": "20261231"}