NDC 76478-501

Nembutal Sodium

Pentobarbital Sodium

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

Product ID76478-501_05af1063-ce0d-485f-a569-3345f6e1b761
NDC76478-501
Product TypeHuman Prescription Drug
Proprietary NameNembutal Sodium
Generic NamePentobarbital Sodium
Dosage FormInjection
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS
Marketing Start Date1973-09-19
Marketing CategoryANDA / ANDA
Application NumberANDA083246
Labeler NameAkron
Substance NamePENTOBARBITAL SODIUM
Active Ingredient Strength50 mg/mL
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 76478-501-20

1 VIAL in 1 CARTON (76478-501-20) > 20 mL in 1 VIAL
Marketing Start Date1973-09-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 76478-501-50 [76478050150]

Nembutal Sodium INJECTION
Marketing CategoryANDA
Application NumberANDA083246
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1973-09-19

NDC 76478-501-20 [76478050120]

Nembutal Sodium INJECTION
Marketing CategoryANDA
Application NumberANDA083246
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1973-09-19

Drug Details

Active Ingredients

IngredientStrength
PENTOBARBITAL SODIUM50 mg/mL

OpenFDA Data

SPL SET ID:5c380ab0-4386-48b6-80ab-ca594b23bc74
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 207468
  • 238090
  • UPC Code
  • 0376478501203
  • NDC Crossover Matching brand name "Nembutal Sodium" or generic name "Pentobarbital Sodium"

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

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