Package 0603-5168-32

Brand: phenobarbital

Generic: phenobarbital
NDC Package

Package Facts

Identity

Package NDC 0603-5168-32
Digits Only 0603516832
Product NDC 0603-5168
Product ID 0603-5168_670a5f53-11d3-4132-b6e5-4ad63852cfa7
Description

1000 TABLET in 1 BOTTLE, PLASTIC (0603-5168-32)

Marketing

Marketing Status
Marketed Since 2001-12-01
Brand phenobarbital
Generic phenobarbital
Sample Package No

Linked Drug Pages (1)

Phenobarbital ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "670a5f53-11d3-4132-b6e5-4ad63852cfa7", "openfda": {"unii": ["YQE403BP4D"], "rxcui": ["198086", "199164", "199167", "199168"], "spl_set_id": ["069b92ce-0061-4724-8c25-08d8596770a2"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0603-5168-21)", "package_ndc": "0603-5168-21", "marketing_start_date": "20011201"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0603-5168-32)", "package_ndc": "0603-5168-32", "marketing_start_date": "20011201"}], "brand_name": "Phenobarbital", "product_id": "0603-5168_670a5f53-11d3-4132-b6e5-4ad63852cfa7", "dosage_form": "TABLET", "product_ndc": "0603-5168", "dea_schedule": "CIV", "generic_name": "phenobarbital", "labeler_name": "Endo USA, 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": "20011201", "listing_expiration_date": "20261231"}