Package 51672-5329-3

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 51672-5329-3
Digits Only 5167253293
Product NDC 51672-5329
Description

1000 TABLET in 1 BOTTLE, PLASTIC (51672-5329-3)

Marketing

Marketing Status
Marketed Since 2024-08-01
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": "bc2d569d-e2c5-4a94-b259-cac1fcc6cdf4", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198083", "198086", "198089", "199164", "199167", "199168", "312357", "312362"], "spl_set_id": ["fa09b4f2-edb0-4594-a2d2-b16f7b9686b4"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A. Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (51672-5329-1)", "package_ndc": "51672-5329-1", "marketing_start_date": "20240801"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (51672-5329-3)", "package_ndc": "51672-5329-3", "marketing_start_date": "20240801"}], "brand_name": "Phenobarbital", "product_id": "51672-5329_bc2d569d-e2c5-4a94-b259-cac1fcc6cdf4", "dosage_form": "TABLET", "product_ndc": "51672-5329", "dea_schedule": "CIV", "generic_name": "Phenobarbital", "labeler_name": "Taro Pharmaceuticals U.S.A. Inc.", "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": "20240801", "listing_expiration_date": "20261231"}