NDC 0781-8940

L-Cysteine Hydrochloride

L-cysteine Hydrochloride

L-Cysteine Hydrochloride is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Sandoz Inc. The primary component is Cysteine Hydrochloride.

Product ID0781-8940_3c24d7cf-21ae-489a-ad2e-b8ff21604bd9
NDC0781-8940
Product TypeHuman Prescription Drug
Proprietary NameL-Cysteine Hydrochloride
Generic NameL-cysteine Hydrochloride
Dosage FormInjection, Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2016-06-14
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameSandoz Inc
Substance NameCYSTEINE HYDROCHLORIDE
Active Ingredient Strength50 mg/mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0781-8940-95

10 VIAL, SINGLE-DOSE in 1 CARTON (0781-8940-95) > 10 mL in 1 VIAL, SINGLE-DOSE (0781-8940-70)
Marketing Start Date2016-06-14
Marketing End Date2021-06-30
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0781-8940-70 [00781894070]

L-Cysteine Hydrochloride INJECTION, SOLUTION
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-06-14
Marketing End Date2021-06-30

NDC 0781-8940-95 [00781894095]

L-Cysteine Hydrochloride INJECTION, SOLUTION
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-06-14
Marketing End Date2021-06-30

Drug Details

Active Ingredients

IngredientStrength
CYSTEINE HYDROCHLORIDE50 mg/mL

OpenFDA Data

SPL SET ID:4595bfbe-c3b5-4053-b6f5-2e2b9ff85c82
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1667993

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