lithium carbonate

Generic: lithium carbonate

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lithium carbonate
Generic Name lithium carbonate
Labeler rising pharma holdings, inc.
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

lithium carbonate 450 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-278
Product ID 64980-278_c2afa358-e66b-48aa-8c51-79b55ac31016
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205663
Listing Expiration 2026-12-31
Marketing Start 2018-03-01

Pharmacologic Class

Classes
mood stabilizer [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64980278
Hyphenated Format 64980-278

Supplemental Identifiers

RxCUI
197892
UNII
2BMD2GNA4V

Packaging Origin

Original Packager
true

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 ANDA205663 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 450 mg/1
source: ndc
Packaging
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-278-01)
source: ndc

Packages (1)

Ingredients (1)

lithium carbonate (450 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c2afa358-e66b-48aa-8c51-79b55ac31016", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197892"], "spl_set_id": ["5e18d105-662d-4729-aa81-00be7472adde"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-278-01)", "package_ndc": "64980-278-01", "marketing_start_date": "20180301"}], "brand_name": "Lithium Carbonate", "product_id": "64980-278_c2afa358-e66b-48aa-8c51-79b55ac31016", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "64980-278", "generic_name": "Lithium Carbonate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "450 mg/1"}], "application_number": "ANDA205663", "marketing_category": "ANDA", "marketing_start_date": "20180301", "listing_expiration_date": "20261231"}