lithium carbonate

Generic: lithium carbonate

Labeler: american health packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium carbonate
Generic Name lithium carbonate
Labeler american health packaging
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

lithium carbonate 300 mg/1

Manufacturer
American Health Packaging

Identifiers & Regulatory

Product NDC 68084-640
Product ID 68084-640_437e7f3e-a3f5-cecd-e063-6294a90ac816
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076832
Listing Expiration 2026-12-31
Marketing Start 2014-10-13

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68084640
Hyphenated Format 68084-640

Supplemental Identifiers

RxCUI
197891
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
  • 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-640-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-640-11)
source: ndc

Packages (1)

Ingredients (1)

lithium carbonate (300 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "437e7f3e-a3f5-cecd-e063-6294a90ac816", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["5ce5ebd2-f1b5-4c04-a7de-56a1b7eb8197"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-640-01)  / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-640-11)", "package_ndc": "68084-640-01", "marketing_start_date": "20141013"}], "brand_name": "Lithium Carbonate", "product_id": "68084-640_437e7f3e-a3f5-cecd-e063-6294a90ac816", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "68084-640", "generic_name": "Lithium Carbonate", "labeler_name": "American Health Packaging", "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": "20141013", "listing_expiration_date": "20261231"}