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Phenobarbital - 63739-201-10 - (Phenobarbital)

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Drug Information of Phenobarbital

Product NDC: 63739-201
Proprietary Name: Phenobarbital
Non Proprietary Name: Phenobarbital
Active Ingredient(s): 32.4    mg/1 & nbsp;   Phenobarbital
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Phenobarbital

Product NDC: 63739-201
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20070717

Package Information of Phenobarbital

Package NDC: 63739-201-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-201-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Phenobarbital

NDC Code 63739-201-10
Proprietary Name Phenobarbital
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-201-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-201
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phenobarbital
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070717
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name PHENOBARBITAL
Strength Number 32.4
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Phenobarbital


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