Package 62559-280-01

Brand: lithobid

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 62559-280-01
Digits Only 6255928001
Product NDC 62559-280
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62559-280-01)

Marketing

Marketing Status
Marketed Since 2014-07-01
Brand lithobid
Generic lithium carbonate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "75db0302-4a60-4b41-85fa-99ff2761ce56", "openfda": {"upc": ["0362559280013"], "unii": ["2BMD2GNA4V"], "rxcui": ["197891", "206786"], "spl_set_id": ["f7f5b69a-c2a1-4586-a189-1475d41387c0"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62559-280-01)", "package_ndc": "62559-280-01", "marketing_start_date": "20140701"}], "brand_name": "LITHOBID", "product_id": "62559-280_75db0302-4a60-4b41-85fa-99ff2761ce56", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "62559-280", "generic_name": "lithium carbonate", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LITHOBID", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "NDA018027", "marketing_category": "NDA", "marketing_start_date": "20140701", "listing_expiration_date": "20261231"}