lithium carbonate
Generic: lithium carbonate
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
lithium carbonate
Generic Name
lithium carbonate
Labeler
american health packaging
Dosage Form
TABLET, EXTENDED RELEASE
Routes
Active Ingredients
lithium carbonate 300 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68084-640
Product ID
68084-640_437e7f3e-a3f5-cecd-e063-6294a90ac816
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076832
Listing Expiration
2026-12-31
Marketing Start
2014-10-13
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68084640
Hyphenated Format
68084-640
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
ANDA076832 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-640-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-640-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "437e7f3e-a3f5-cecd-e063-6294a90ac816", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["5ce5ebd2-f1b5-4c04-a7de-56a1b7eb8197"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-640-01) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-640-11)", "package_ndc": "68084-640-01", "marketing_start_date": "20141013"}], "brand_name": "Lithium Carbonate", "product_id": "68084-640_437e7f3e-a3f5-cecd-e063-6294a90ac816", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "68084-640", "generic_name": "Lithium Carbonate", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA076832", "marketing_category": "ANDA", "marketing_start_date": "20141013", "listing_expiration_date": "20261231"}