Package 70752-163-14

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 70752-163-14
Digits Only 7075216314
Product NDC 70752-163
Description

500 TABLET in 1 BOTTLE (70752-163-14)

Marketing

Marketing Status
Marketed Since 2020-09-15
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": "234e0cf8-e1c9-47a2-8fa3-8a4db929c866", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198086", "199164", "199167", "199168"], "spl_set_id": ["7e6853a4-478d-40e3-b041-4cff02a74c8c"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70752-163-10)", "package_ndc": "70752-163-10", "marketing_start_date": "20200915"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (70752-163-11)", "package_ndc": "70752-163-11", "marketing_start_date": "20200915"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70752-163-14)", "package_ndc": "70752-163-14", "marketing_start_date": "20200915"}], "brand_name": "PHENOBARBITAL", "product_id": "70752-163_234e0cf8-e1c9-47a2-8fa3-8a4db929c866", "dosage_form": "TABLET", "product_ndc": "70752-163", "dea_schedule": "CIV", "generic_name": "PHENOBARBITAL", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "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": "20200915", "listing_expiration_date": "20261231"}