Package 70518-4215-0
Brand: phenobarbital
Generic: phenobarbitalPackage Facts
Identity
Package NDC
70518-4215-0
Digits Only
7051842150
Product NDC
70518-4215
Description
30 TABLET in 1 BLISTER PACK (70518-4215-0)
Marketing
Marketing Status
Brand
phenobarbital
Generic
phenobarbital
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ff6e91a-3b9a-9070-e063-6394a90a8779", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["199168"], "spl_set_id": ["4e6f2a3b-c6e2-488e-827a-e8646279532d"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4215-0)", "package_ndc": "70518-4215-0", "marketing_start_date": "20241016"}], "brand_name": "Phenobarbital", "product_id": "70518-4215_3ff6e91a-3b9a-9070-e063-6394a90a8779", "dosage_form": "TABLET", "product_ndc": "70518-4215", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "64.8 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20241016", "listing_expiration_date": "20261231"}