lithium carbonate
Generic: lithium carbonate
Labeler: ncs healthcare of ky, llc dba vangard labsDrug Facts
Product Profile
Brand Name
lithium carbonate
Generic Name
lithium carbonate
Labeler
ncs healthcare of ky, llc dba vangard labs
Dosage Form
CAPSULE
Routes
Active Ingredients
lithium carbonate 300 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0615-8480
Product ID
0615-8480_01fffc2d-591d-4a52-b659-7837eabd163a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079139
Listing Expiration
2026-12-31
Marketing Start
2009-02-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06158480
Hyphenated Format
0615-8480
Supplemental Identifiers
RxCUI
UNII
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
ANDA079139 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
Packaging
- 30 CAPSULE in 1 BLISTER PACK (0615-8480-39)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "01fffc2d-591d-4a52-b659-7837eabd163a", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197889"], "spl_set_id": ["204d94de-83e4-400e-bd6b-70b49813802c"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (0615-8480-39)", "package_ndc": "0615-8480-39", "marketing_start_date": "20230821"}], "brand_name": "Lithium Carbonate", "product_id": "0615-8480_01fffc2d-591d-4a52-b659-7837eabd163a", "dosage_form": "CAPSULE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "0615-8480", "generic_name": "Lithium Carbonate", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA079139", "marketing_category": "ANDA", "marketing_start_date": "20090203", "listing_expiration_date": "20261231"}