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Phenobarbital - 17856-1508-2 - (phenobarbital)

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Drug Information of Phenobarbital

Product NDC: 17856-1508
Proprietary Name: Phenobarbital
Non Proprietary Name: phenobarbital
Active Ingredient(s): 20    mg/5mL & nbsp;   phenobarbital
Administration Route(s): ORAL
Dosage Form(s): ELIXIR
Coding System: National Drug Codes(NDC)

Labeler Information of Phenobarbital

Product NDC: 17856-1508
Labeler Name: Atlantic Biologicals Corps
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19970101

Package Information of Phenobarbital

Package NDC: 17856-1508-2
Package Description: 7.5 mL in 1 CUP (17856-1508-2)

NDC Information of Phenobarbital

NDC Code 17856-1508-2
Proprietary Name Phenobarbital
Package Description 7.5 mL in 1 CUP (17856-1508-2)
Product NDC 17856-1508
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name phenobarbital
Dosage Form Name ELIXIR
Route Name ORAL
Start Marketing Date 19970101
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Atlantic Biologicals Corps
Substance Name PHENOBARBITAL
Strength Number 20
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Phenobarbital


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