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Nutropin AQ - 50242-022-20 - (somatropin (rDNA origin))

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Drug Information of Nutropin AQ

Product NDC: 50242-022
Proprietary Name: Nutropin AQ
Non Proprietary Name: somatropin (rDNA origin)
Active Ingredient(s): 10    mg/2mL & nbsp;   somatropin (rDNA origin)
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nutropin AQ

Product NDC: 50242-022
Labeler Name: Genentech, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020522
Marketing Category: NDA
Start Marketing Date: 19951229

Package Information of Nutropin AQ

Package NDC: 50242-022-20
Package Description: 1 VIAL in 1 CARTON (50242-022-20) > 2 mL in 1 VIAL

NDC Information of Nutropin AQ

NDC Code 50242-022-20
Proprietary Name Nutropin AQ
Package Description 1 VIAL in 1 CARTON (50242-022-20) > 2 mL in 1 VIAL
Product NDC 50242-022
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name somatropin (rDNA origin)
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 19951229
Marketing Category Name NDA
Labeler Name Genentech, Inc.
Substance Name SOMATROPIN
Strength Number 10
Strength Unit mg/2mL
Pharmaceutical Classes Recombinant Human Growth Hormone [EPC],Recombinant Human Growth Hormones [Chemical/Ingredient]

Complete Information of Nutropin AQ


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