lithium carbonate
Generic: lithium carbonate
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
lithium carbonate
Generic Name
lithium carbonate
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE, GELATIN COATED
Routes
Active Ingredients
lithium carbonate 300 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-173
Product ID
72789-173_40a77b87-bcf9-bcb1-e063-6294a90ad29a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA017812
Listing Expiration
2026-12-31
Marketing Start
1980-11-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789173
Hyphenated Format
72789-173
Supplemental Identifiers
RxCUI
UPC
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
NDA017812 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 300 mg/1
Packaging
- 100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (72789-173-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40a77b87-bcf9-bcb1-e063-6294a90ad29a", "openfda": {"upc": ["0372789173016"], "unii": ["2BMD2GNA4V"], "rxcui": ["197889"], "spl_set_id": ["c4973d87-d014-42f4-ba13-ae628ca1a451"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (72789-173-01)", "package_ndc": "72789-173-01", "marketing_start_date": "20210309"}], "brand_name": "Lithium Carbonate", "product_id": "72789-173_40a77b87-bcf9-bcb1-e063-6294a90ad29a", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "72789-173", "generic_name": "Lithium Carbonate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "NDA017812", "marketing_category": "NDA", "marketing_start_date": "19801126", "listing_expiration_date": "20261231"}