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L-Cysteine Hydrochloride - 66758-005-02 - (L-Cysteine Hydrochloride)

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Drug Information of L-Cysteine Hydrochloride

Product NDC: 66758-005
Proprietary Name: L-Cysteine Hydrochloride
Non Proprietary Name: L-Cysteine Hydrochloride
Active Ingredient(s): 50    mg/mL & nbsp;   L-Cysteine Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of L-Cysteine Hydrochloride

Product NDC: 66758-005
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20081201

Package Information of L-Cysteine Hydrochloride

Package NDC: 66758-005-02
Package Description: 5 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (66758-005-02) > 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (66758-005-01)

NDC Information of L-Cysteine Hydrochloride

NDC Code 66758-005-02
Proprietary Name L-Cysteine Hydrochloride
Package Description 5 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (66758-005-02) > 50 mL in 1 VIAL, PHARMACY BULK PACKAGE (66758-005-01)
Product NDC 66758-005
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name L-Cysteine Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20081201
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Sandoz Inc
Substance Name CYSTEINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of L-Cysteine Hydrochloride


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