lithium carbonate er
Generic: lithium carbonate
Labeler: avkareDrug Facts
Product Profile
Brand Name
lithium carbonate er
Generic Name
lithium carbonate
Labeler
avkare
Dosage Form
TABLET
Routes
Active Ingredients
lithium carbonate 450 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42291-496
Product ID
42291-496_485f83f8-8405-eae8-e063-6294a90a3c33
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA091616
Listing Expiration
2027-12-31
Marketing Start
2022-02-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42291496
Hyphenated Format
42291-496
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 er (source: ndc)
Generic Name
lithium carbonate (source: ndc)
Application Number
ANDA091616 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 450 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (42291-496-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "485f83f8-8405-eae8-e063-6294a90a3c33", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197892"], "spl_set_id": ["d8ddff4d-2b77-a8f2-e053-2a95a90a5fc0"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42291-496-01)", "package_ndc": "42291-496-01", "marketing_start_date": "20220225"}], "brand_name": "Lithium Carbonate ER", "product_id": "42291-496_485f83f8-8405-eae8-e063-6294a90a3c33", "dosage_form": "TABLET", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "42291-496", "generic_name": "Lithium Carbonate", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "brand_name_suffix": "ER", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "450 mg/1"}], "application_number": "ANDA091616", "marketing_category": "ANDA", "marketing_start_date": "20220225", "listing_expiration_date": "20271231"}