lithobid
Generic: lithium carbonate
Labeler: ani pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
lithobid
Generic Name
lithium carbonate
Labeler
ani pharmaceuticals, inc.
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Routes
Active Ingredients
lithium carbonate 300 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
62559-280
Product ID
62559-280_75db0302-4a60-4b41-85fa-99ff2761ce56
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018027
Listing Expiration
2026-12-31
Marketing Start
2014-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
62559280
Hyphenated Format
62559-280
Supplemental Identifiers
RxCUI
UPC
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
lithobid (source: ndc)
Generic Name
lithium carbonate (source: ndc)
Application Number
NDA018027 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
Packaging
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62559-280-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "75db0302-4a60-4b41-85fa-99ff2761ce56", "openfda": {"upc": ["0362559280013"], "unii": ["2BMD2GNA4V"], "rxcui": ["197891", "206786"], "spl_set_id": ["f7f5b69a-c2a1-4586-a189-1475d41387c0"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62559-280-01)", "package_ndc": "62559-280-01", "marketing_start_date": "20140701"}], "brand_name": "LITHOBID", "product_id": "62559-280_75db0302-4a60-4b41-85fa-99ff2761ce56", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "62559-280", "generic_name": "lithium carbonate", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LITHOBID", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "NDA018027", "marketing_category": "NDA", "marketing_start_date": "20140701", "listing_expiration_date": "20261231"}