Package 63629-1035-1

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 63629-1035-1
Digits Only 6362910351
Product NDC 63629-1035
Description

1000 TABLET in 1 BOTTLE, PLASTIC (63629-1035-1)

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": "5f85d98e-af91-4bd4-82e8-adc7589ed8f1", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["199167"], "spl_set_id": ["cf0cc3bf-23ba-42a5-8d0c-5d9aec443429"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (63629-1035-1)", "package_ndc": "63629-1035-1", "marketing_start_date": "20221109"}], "brand_name": "Phenobarbital", "product_id": "63629-1035_5f85d98e-af91-4bd4-82e8-adc7589ed8f1", "dosage_form": "TABLET", "product_ndc": "63629-1035", "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": "32.4 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20141124", "listing_expiration_date": "20261231"}