NDC 0781-6021

DILUENT

Water Solution

DILUENT is a Intravenous; Subcutaneous Injection in the Human Prescription Drug category. It is labeled and distributed by Sandoz Inc. The primary component is Water.

Product ID0781-6021_19f50f18-7400-4b9f-b97a-49b16c48b207
NDC0781-6021
Product TypeHuman Prescription Drug
Proprietary NameDILUENT
Generic NameWater Solution
Dosage FormInjection
Route of AdministrationINTRAVENOUS; SUBCUTANEOUS
Marketing Start Date2019-03-25
Marketing CategoryANDA / ANDA
Application NumberANDA203649
Labeler NameSandoz Inc
Substance NameWATER
Active Ingredient Strength1 mL/mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 0781-6021-94

1 VIAL in 1 CARTON (0781-6021-94) > 50 mL in 1 VIAL
Marketing Start Date2019-03-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0781-6021-94 [00781602194]

DILUENT INJECTION
Marketing CategoryANDA
Application NumberANDA203649
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2019-03-25

Drug Details

Active Ingredients

IngredientStrength
WATER1 mL/mL

OpenFDA Data

SPL SET ID:473297ca-a872-4052-a053-87dc8f0d3c13
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 349408
  • 349409
  • 349410
  • 349407
  • NDC Crossover Matching brand name "DILUENT" or generic name "Water Solution"

    NDCBrand NameGeneric Name
    0173-0518Diluentwater
    0173-0857Diluentwater
    0781-6021DILUENTwater solution
    49281-912DiluentSodium Chloride
    24208-005Advanced Eye Relief Eye Washwater solution
    73408-936Crane Safety Eye Washwater solution
    30142-010Eye Washwater solution
    0002-0800Sterile Diluentdiluent

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