Package 70518-2226-0

Brand: buprenorphine hcl

Generic: buprenorphine hcl
NDC Package

Package Facts

Identity

Package NDC 70518-2226-0
Digits Only 7051822260
Product NDC 70518-2226
Product ID 70518-2226_49ed3641-911e-6046-e063-6394a90a0304
Description

30 TABLET in 1 BLISTER PACK (70518-2226-0)

Marketing

Marketing Status
Marketed Since 2019-07-19
Brand buprenorphine hcl
Generic buprenorphine hcl
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBLINGUAL"], "spl_id": "49ed3641-911e-6046-e063-6394a90a0304", "openfda": {"unii": ["56W8MW3EN1"], "rxcui": ["351264"], "spl_set_id": ["e1aac2bb-cb83-46cb-9a29-502a62010667"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2226-0)", "package_ndc": "70518-2226-0", "marketing_start_date": "20190719"}], "brand_name": "Buprenorphine HCl", "product_id": "70518-2226_49ed3641-911e-6046-e063-6394a90a0304", "dosage_form": "TABLET", "pharm_class": ["Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "70518-2226", "dea_schedule": "CIII", "generic_name": "Buprenorphine HCl", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buprenorphine HCl", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA078633", "marketing_category": "ANDA", "marketing_start_date": "20190719", "listing_expiration_date": "20271231"}