Package 70518-2312-0

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 70518-2312-0
Digits Only 7051823120
Product NDC 70518-2312
Product ID 70518-2312_4a00cc60-1f0b-8fa8-e063-6294a90a567b
Description

100 POUCH in 1 BOX (70518-2312-0) / 1 CAPSULE in 1 POUCH (70518-2312-1)

Marketing

Marketing Status
Marketed Since 2019-09-13
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": "4a00cc60-1f0b-8fa8-e063-6294a90a567b", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197893"], "spl_set_id": ["803eab29-0d0a-4df0-b504-bcd85ec01ead"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-2312-0)  / 1 CAPSULE in 1 POUCH (70518-2312-1)", "package_ndc": "70518-2312-0", "marketing_start_date": "20190913"}], "brand_name": "Lithium Carbonate", "product_id": "70518-2312_4a00cc60-1f0b-8fa8-e063-6294a90a567b", "dosage_form": "CAPSULE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "70518-2312", "generic_name": "Lithium Carbonate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "600 mg/1"}], "application_number": "ANDA079139", "marketing_category": "ANDA", "marketing_start_date": "20190913", "listing_expiration_date": "20271231"}