NDC 60267-311

Sodium Nitrite

Sodium Nitrite

Sodium Nitrite is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hope Pharmaceuticals. The primary component is Sodium Nitrite.

Product ID60267-311_28c24f53-7fe4-4607-99b7-fdebd7bc3ad1
NDC60267-311
Product TypeHuman Prescription Drug
Proprietary NameSodium Nitrite
Generic NameSodium Nitrite
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2012-02-14
Marketing CategoryNDA / NDA
Application NumberNDA203922
Labeler NameHope Pharmaceuticals
Substance NameSODIUM NITRITE
Active Ingredient Strength30 mg/mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 60267-311-10

10 mL in 1 VIAL, SINGLE-USE (60267-311-10)
Marketing Start Date2012-02-14
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 60267-311-10 [60267031110]

Sodium Nitrite INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA203922
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2012-02-14

Drug Details

Active Ingredients

IngredientStrength
SODIUM NITRITE30 mg/mL

OpenFDA Data

SPL SET ID:52f01c6e-172a-47a9-98a6-9eab7651a032
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 253010

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