Package 70518-1713-0

Brand: diazepam

Generic: diazepam
NDC Package

Package Facts

Identity

Package NDC 70518-1713-0
Digits Only 7051817130
Product NDC 70518-1713
Product ID 70518-1713_49617f72-cc27-7c0d-e063-6294a90ac558
Description

30 TABLET in 1 BLISTER PACK (70518-1713-0)

Marketing

Marketing Status
Marketed Since 2018-12-06
Brand diazepam
Generic diazepam
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49617f72-cc27-7c0d-e063-6294a90ac558", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197591"], "spl_set_id": ["20e08b97-bb89-4129-a228-8ad9cf35a1d3"], "pharm_class_cs": ["Benzodiazepines [CS]"], "pharm_class_epc": ["Benzodiazepine [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1713-0)", "package_ndc": "70518-1713-0", "marketing_start_date": "20181206"}], "brand_name": "Diazepam", "product_id": "70518-1713_49617f72-cc27-7c0d-e063-6294a90ac558", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70518-1713", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "5 mg/1"}], "application_number": "ANDA071321", "marketing_category": "ANDA", "marketing_start_date": "20181206", "listing_expiration_date": "20271231"}