Package 70518-0608-0

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 70518-0608-0
Digits Only 7051806080
Product NDC 70518-0608
Product ID 70518-0608_47fa78bf-bc42-7178-e063-6394a90a8719
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-0608-0)

Marketing

Marketing Status
Marketed Since 2017-07-06
Brand lithium carbonate
Generic lithium carbonate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "47fa78bf-bc42-7178-e063-6394a90a8719", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197891"], "spl_set_id": ["611b0ea2-6378-4c8f-953d-87f6b35b0634"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-0608-0)", "package_ndc": "70518-0608-0", "marketing_start_date": "20170706"}], "brand_name": "Lithium Carbonate", "product_id": "70518-0608_47fa78bf-bc42-7178-e063-6394a90a8719", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "70518-0608", "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": "ANDA204779", "marketing_category": "ANDA", "marketing_start_date": "20170706", "listing_expiration_date": "20271231"}