NDC 0187-4303

Amytal Sodium

Amobarbital Sodium

Amytal Sodium is a Intramuscular; Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Bausch Health Us Llc. The primary component is Amobarbital Sodium.

Product ID0187-4303_712a7960-f90e-4db4-9566-2c4e3be83d0e
NDC0187-4303
Product TypeHuman Prescription Drug
Proprietary NameAmytal Sodium
Generic NameAmobarbital Sodium
Dosage FormInjection, Powder, Lyophilized, For Solution
Route of AdministrationINTRAMUSCULAR; INTRAVENOUS
Marketing Start Date2008-09-25
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameBausch Health US LLC
Substance NameAMOBARBITAL SODIUM
Active Ingredient Strength1 g/5mL
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0187-4303-05

5 mL in 1 VIAL, GLASS (0187-4303-05)
Marketing Start Date2008-09-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0187-4303-05 [00187430305]

Amytal Sodium INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2008-09-25

Drug Details

Active Ingredients

IngredientStrength
AMOBARBITAL SODIUM.5 g/5mL

OpenFDA Data

SPL SET ID:a2523317-e071-4e04-9d9f-9053286e0ce2
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 201628
  • 308170

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