NDC 17478-181

Pentobarbital Sodium

Pentobarbital Sodium

Pentobarbital Sodium is a Intramuscular; Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Akorn, Inc.. The primary component is Pentobarbital Sodium.

Product ID17478-181_33c29644-348a-4e8f-8429-640b83e363c8
NDC17478-181
Product TypeHuman Prescription Drug
Proprietary NamePentobarbital Sodium
Generic NamePentobarbital Sodium
Dosage FormInjection
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS
Marketing Start Date2019-01-17
Marketing CategoryANDA / ANDA
Application NumberANDA083246
Labeler NameAkorn, Inc.
Substance NamePENTOBARBITAL SODIUM
Active Ingredient Strength50 mg/mL
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 17478-181-20

1 VIAL, MULTI-DOSE in 1 CARTON (17478-181-20) > 20 mL in 1 VIAL, MULTI-DOSE
Marketing Start Date2019-01-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 17478-181-50 [17478018150]

Pentobarbital Sodium INJECTION
Marketing CategoryANDA
Application NumberANDA083246
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-01-17

NDC 17478-181-20 [17478018120]

Pentobarbital Sodium INJECTION
Marketing CategoryANDA
Application NumberANDA083246
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-01-17

Drug Details

Active Ingredients

IngredientStrength
PENTOBARBITAL SODIUM50 mg/mL

OpenFDA Data

SPL SET ID:0a202fdc-0dc0-4b1a-b858-886914d27c85
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 238090
    • UPC Code
  • 0317478181200

    • NDC Crossover Matching brand name "Pentobarbital Sodium" or generic name "Pentobarbital Sodium"

    NDCBrand NameGeneric Name
    17478-181Pentobarbital SodiumPentobarbital Sodium
    24201-010Pentobarbital SodiumPentobarbital Sodium
    25021-676pentobarbital sodiumpentobarbital sodium
    70655-501Pentobarbital Sodiumpentobarbital sodium
    76478-501Nembutal Sodiumpentobarbital sodium
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