Package 70518-0162-0

Brand: diazepam

Generic: diazepam
NDC Package

Package Facts

Identity

Package NDC 70518-0162-0
Digits Only 7051801620
Product NDC 70518-0162
Product ID 70518-0162_4b1e1881-5865-403c-e063-6294a90af3d9
Description

30 TABLET in 1 BLISTER PACK (70518-0162-0)

Marketing

Marketing Status
Marketed Since 2017-01-23
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": "4b1e1881-5865-403c-e063-6294a90af3d9", "openfda": {"nui": ["N0000175694", "M0002356"], "unii": ["Q3JTX2Q7TU"], "rxcui": ["197589"], "spl_set_id": ["5ebef149-1858-4199-aaed-7b9341fae63d"], "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 (70518-0162-0)", "package_ndc": "70518-0162-0", "marketing_start_date": "20170123"}], "brand_name": "Diazepam", "product_id": "70518-0162_4b1e1881-5865-403c-e063-6294a90af3d9", "dosage_form": "TABLET", "pharm_class": ["Benzodiazepine [EPC]", "Benzodiazepines [CS]"], "product_ndc": "70518-0162", "dea_schedule": "CIV", "generic_name": "Diazepam", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Diazepam", "active_ingredients": [{"name": "DIAZEPAM", "strength": "10 mg/1"}], "application_number": "ANDA071322", "marketing_category": "ANDA", "marketing_start_date": "20170123", "listing_expiration_date": "20271231"}