Package 70518-0668-1

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 70518-0668-1
Digits Only 7051806681
Product NDC 70518-0668
Product ID 70518-0668_47fab62b-30fd-0be2-e063-6294a90a1769
Description

30 CAPSULE in 1 BLISTER PACK (70518-0668-1)

Marketing

Marketing Status
Marketed Since 2023-12-19
Brand lithium carbonate
Generic lithium carbonate
Sample Package No

Linked Drug Pages (1)

Lithium Carbonate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47fab62b-30fd-0be2-e063-6294a90a1769", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197889"], "spl_set_id": ["1c320bff-b4d5-42f2-b2b5-238564fe9589"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-0668-1)", "package_ndc": "70518-0668-1", "marketing_start_date": "20231219"}], "brand_name": "Lithium Carbonate", "product_id": "70518-0668_47fab62b-30fd-0be2-e063-6294a90a1769", "dosage_form": "CAPSULE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "70518-0668", "generic_name": "Lithium Carbonate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "300 mg/1"}], "application_number": "ANDA079139", "marketing_category": "ANDA", "marketing_start_date": "20170810", "listing_expiration_date": "20271231"}