NDC 25021-676

pentobarbital sodium

Pentobarbital Sodium

pentobarbital sodium is a Intramuscular; Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Sagent Pharmaceuticals. The primary component is Pentobarbital Sodium.

Product ID25021-676_5eb44748-b3d4-4d86-a172-9f03eb804671
NDC25021-676
Product TypeHuman Prescription Drug
Proprietary Namepentobarbital sodium
Generic NamePentobarbital Sodium
Dosage FormInjection, Solution
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS
Marketing Start Date2017-04-19
Marketing CategoryANDA / ANDA
Application NumberANDA206404
Labeler NameSagent Pharmaceuticals
Substance NamePENTOBARBITAL SODIUM
Active Ingredient Strength50 mg/mL
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 25021-676-20

1 VIAL in 1 CARTON (25021-676-20) > 20 mL in 1 VIAL
Marketing Start Date2017-04-19
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 25021-676-50 [25021067650]

pentobarbital sodium INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA206404
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2017-04-19

NDC 25021-676-20 [25021067620]

pentobarbital sodium INJECTION, SOLUTION
Marketing CategoryANDA
Application NumberANDA206404
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2017-04-19

Drug Details

Active Ingredients

IngredientStrength
PENTOBARBITAL SODIUM50 mg/mL

OpenFDA Data

SPL SET ID:e9f4b344-b092-4eec-b49d-d8cfe8ebc05d
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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