Package 72789-173-01

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 72789-173-01
Digits Only 7278917301
Product NDC 72789-173
Description

100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (72789-173-01)

Marketing

Marketing Status
Marketed Since 2021-03-09
Brand lithium carbonate
Generic lithium carbonate
Sample Package No

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"}