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PHENYTOIN SODIUM - 39822-4050-3 - (PHENYTOIN SODIUM)

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Drug Information of PHENYTOIN SODIUM

Product NDC: 39822-4050
Proprietary Name: PHENYTOIN SODIUM
Non Proprietary Name: PHENYTOIN SODIUM
Active Ingredient(s): 50    mg/mL & nbsp;   PHENYTOIN SODIUM
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of PHENYTOIN SODIUM

Product NDC: 39822-4050
Labeler Name: X-GEN Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040573
Marketing Category: ANDA
Start Marketing Date: 20110502

Package Information of PHENYTOIN SODIUM

Package NDC: 39822-4050-3
Package Description: 25 VIAL, SINGLE-DOSE in 1 CARTON (39822-4050-3) > 2 mL in 1 VIAL, SINGLE-DOSE (39822-4050-2)

NDC Information of PHENYTOIN SODIUM

NDC Code 39822-4050-3
Proprietary Name PHENYTOIN SODIUM
Package Description 25 VIAL, SINGLE-DOSE in 1 CARTON (39822-4050-3) > 2 mL in 1 VIAL, SINGLE-DOSE (39822-4050-2)
Product NDC 39822-4050
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PHENYTOIN SODIUM
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110502
Marketing Category Name ANDA
Labeler Name X-GEN Pharmaceuticals, Inc.
Substance Name PHENYTOIN SODIUM
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]

Complete Information of PHENYTOIN SODIUM


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