lithium carbonate
Generic: lithium carbonate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
lithium carbonate
Generic Name
lithium carbonate
Labeler
remedyrepack inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
lithium carbonate 150 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3565
Product ID
70518-3565_3c56e37f-02b2-0c0f-e063-6394a90a7b3a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079139
Listing Expiration
2026-12-31
Marketing Start
2022-10-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183565
Hyphenated Format
70518-3565
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
- 150 mg/1
Packaging
- 30 CAPSULE in 1 BLISTER PACK (70518-3565-0)
- 100 POUCH in 1 BOX (70518-3565-1) / 1 CAPSULE in 1 POUCH (70518-3565-2)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3c56e37f-02b2-0c0f-e063-6394a90a7b3a", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["311355"], "spl_set_id": ["57faf0b0-4380-4bbf-8de7-c3f9d74fc410"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-3565-0)", "package_ndc": "70518-3565-0", "marketing_start_date": "20221031"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-3565-1) / 1 CAPSULE in 1 POUCH (70518-3565-2)", "package_ndc": "70518-3565-1", "marketing_start_date": "20230928"}], "brand_name": "Lithium Carbonate", "product_id": "70518-3565_3c56e37f-02b2-0c0f-e063-6394a90a7b3a", "dosage_form": "CAPSULE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "70518-3565", "generic_name": "Lithium Carbonate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "150 mg/1"}], "application_number": "ANDA079139", "marketing_category": "ANDA", "marketing_start_date": "20221031", "listing_expiration_date": "20261231"}