lithium carbonate
Generic: lithium carbonate
Labeler: rising pharma holdings, inc.Drug Facts
Product Profile
Brand Name
lithium carbonate
Generic Name
lithium carbonate
Labeler
rising pharma holdings, inc.
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
lithium carbonate 450 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
64980278
Hyphenated Format
64980-278
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 450 mg/1
Packaging
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (64980-278-01)
Packages (1)
Ingredients (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"}