Package 70518-4129-0

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 70518-4129-0
Digits Only 7051841290
Product NDC 70518-4129
Product ID 70518-4129_3fa56bec-cf88-ce76-e063-6294a90ae2bb
Description

30 TABLET in 1 BLISTER PACK (70518-4129-0)

Marketing

Marketing Status
Marketed Since 2024-07-01
Brand phenobarbital
Generic phenobarbital
Sample Package No

Linked Drug Pages (1)

Phenobarbital ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3fa56bec-cf88-ce76-e063-6294a90ae2bb", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["199167"], "spl_set_id": ["4e2910f2-173d-4b5c-aad3-44f4ab40d8cb"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4129-0)", "package_ndc": "70518-4129-0", "marketing_start_date": "20240701"}], "brand_name": "Phenobarbital", "product_id": "70518-4129_3fa56bec-cf88-ce76-e063-6294a90ae2bb", "dosage_form": "TABLET", "product_ndc": "70518-4129", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "32.4 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20240701", "listing_expiration_date": "20261231"}