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Phenobarbital - 63629-4026-1 - (Phenobarbital)

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Drug Information of Phenobarbital

Product NDC: 63629-4026
Proprietary Name: Phenobarbital
Non Proprietary Name: Phenobarbital
Active Ingredient(s): 15    mg/1 & nbsp;   Phenobarbital
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Phenobarbital

Product NDC: 63629-4026
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20000101

Package Information of Phenobarbital

Package NDC: 63629-4026-1
Package Description: 30 TABLET in 1 BOTTLE (63629-4026-1)

NDC Information of Phenobarbital

NDC Code 63629-4026-1
Proprietary Name Phenobarbital
Package Description 30 TABLET in 1 BOTTLE (63629-4026-1)
Product NDC 63629-4026
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phenobarbital
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Bryant Ranch Prepack
Substance Name PHENOBARBITAL
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Phenobarbital


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