Package 70518-2086-0

Brand: lithium carbonate

Generic: lithium carbonate
NDC Package

Package Facts

Identity

Package NDC 70518-2086-0
Digits Only 7051820860
Product NDC 70518-2086
Product ID 70518-2086_499db2fe-4805-e2f7-e063-6394a90ab068
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2086-0)

Marketing

Marketing Status
Marketed Since 2019-05-16
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": "499db2fe-4805-e2f7-e063-6394a90ab068", "openfda": {"unii": ["2BMD2GNA4V"], "rxcui": ["197892"], "spl_set_id": ["db3dc13f-d532-4fcd-a235-c9efab9e6bd7"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2086-0)", "package_ndc": "70518-2086-0", "marketing_start_date": "20190516"}], "brand_name": "Lithium Carbonate", "product_id": "70518-2086_499db2fe-4805-e2f7-e063-6394a90ab068", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Mood Stabilizer [EPC]"], "product_ndc": "70518-2086", "generic_name": "Lithium Carbonate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lithium Carbonate", "active_ingredients": [{"name": "LITHIUM CARBONATE", "strength": "450 mg/1"}], "application_number": "ANDA205663", "marketing_category": "ANDA", "marketing_start_date": "20190516", "listing_expiration_date": "20271231"}