NDC 70655-501

Pentobarbital Sodium

Pentobarbital Sodium

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

Product ID70655-501_2797ced2-5af3-4497-bf28-a0e923118644
NDC70655-501
Product TypeHuman Prescription Drug
Proprietary NamePentobarbital Sodium
Generic NamePentobarbital Sodium
Dosage FormInjection
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS
Marketing Start Date2019-12-28
Marketing CategoryANDA / ANDA
Application NumberANDA206677
Labeler NameRenaissance SSA, LLC
Substance NamePENTOBARBITAL SODIUM
Active Ingredient Strength50 mg/mL
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 70655-501-50

1 VIAL in 1 CARTON (70655-501-50) > 50 mL in 1 VIAL
Marketing Start Date2019-12-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 70655-501-20 [70655050120]

Pentobarbital Sodium INJECTION
Marketing CategoryANDA
Application NumberANDA206677
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-28

NDC 70655-501-50 [70655050150]

Pentobarbital Sodium INJECTION
Marketing CategoryANDA
Application NumberANDA206677
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-12-28

Drug Details

Active Ingredients

IngredientStrength
PENTOBARBITAL SODIUM50 mg/mL

OpenFDA Data

SPL SET ID:a4e701a6-5086-4d47-8972-f5f01b659b10
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 238090

    • 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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