Package 63629-1039-1

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 63629-1039-1
Digits Only 6362910391
Product NDC 63629-1039
Description

1000 TABLET in 1 BOTTLE, PLASTIC (63629-1039-1)

Marketing

Marketing Status
Marketed Since 2022-11-09
Brand phenobarbital
Generic phenobarbital
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b5197fe1-bf14-4aef-aeb1-9bd0d02e1c92", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["199164"], "spl_set_id": ["5aab86ac-4f1b-4494-8c31-f862ac17ec41"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (63629-1039-1)", "package_ndc": "63629-1039-1", "marketing_start_date": "20221109"}], "brand_name": "Phenobarbital", "product_id": "63629-1039_b5197fe1-bf14-4aef-aeb1-9bd0d02e1c92", "dosage_form": "TABLET", "product_ndc": "63629-1039", "dea_schedule": "CIV", "generic_name": "phenobarbital", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Phenobarbital", "active_ingredients": [{"name": "PHENOBARBITAL", "strength": "97.2 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20141124", "listing_expiration_date": "20261231"}