Package 50090-6052-0
Brand: lithium carbonate
Generic: lithium carbonatePackage Facts
Identity
Package NDC
50090-6052-0
Digits Only
5009060520
Product NDC
50090-6052
Description
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6052-0)
Marketing
Marketing Status
Brand
lithium carbonate
Generic
lithium carbonate
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8ac2ae66-bcdc-417a-a8c5-7070d7acadb2", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["baf59ee7-1c98-4f77-96c5-7b50b7acb8f4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6052-0)", "package_ndc": "50090-6052-0", "marketing_start_date": "20220823"}], "brand_name": "Lithium Carbonate", "product_id": "50090-6052_8ac2ae66-bcdc-417a-a8c5-7070d7acadb2", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "50090-6052", "generic_name": "lithium carbonate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA202288", "marketing_category": "ANDA", "marketing_start_date": "20120702", "listing_expiration_date": "20261231"}