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Nembutal Sodium - 76478-501-20 - (pentobarbital sodium)

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Drug Information of Nembutal Sodium

Product NDC: 76478-501
Proprietary Name: Nembutal Sodium
Non Proprietary Name: pentobarbital sodium
Active Ingredient(s): 50    mg/mL & nbsp;   pentobarbital sodium
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nembutal Sodium

Product NDC: 76478-501
Labeler Name: Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.)
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA083246
Marketing Category: ANDA
Start Marketing Date: 19730919

Package Information of Nembutal Sodium

Package NDC: 76478-501-20
Package Description: 1 VIAL in 1 CARTON (76478-501-20) > 20 mL in 1 VIAL

NDC Information of Nembutal Sodium

NDC Code 76478-501-20
Proprietary Name Nembutal Sodium
Package Description 1 VIAL in 1 CARTON (76478-501-20) > 20 mL in 1 VIAL
Product NDC 76478-501
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pentobarbital sodium
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19730919
Marketing Category Name ANDA
Labeler Name Oak Pharmaceuticals, Inc. (Subsidiary of Akorn, Inc.)
Substance Name PENTOBARBITAL SODIUM
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Nembutal Sodium


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