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DELATESTRYL - 67979-501-40 - (TESTOSTERONE ENANTHATE)

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Drug Information of DELATESTRYL

Product NDC: 67979-501
Proprietary Name: DELATESTRYL
Non Proprietary Name: TESTOSTERONE ENANTHATE
Active Ingredient(s): 200    mg/mL & nbsp;   TESTOSTERONE ENANTHATE
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of DELATESTRYL

Product NDC: 67979-501
Labeler Name: Endo Pharmaceuticals Solutions Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA009165
Marketing Category: NDA
Start Marketing Date: 19531224

Package Information of DELATESTRYL

Package NDC: 67979-501-40
Package Description: 1 VIAL, MULTI-DOSE in 1 BOX (67979-501-40) > 5 mL in 1 VIAL, MULTI-DOSE

NDC Information of DELATESTRYL

NDC Code 67979-501-40
Proprietary Name DELATESTRYL
Package Description 1 VIAL, MULTI-DOSE in 1 BOX (67979-501-40) > 5 mL in 1 VIAL, MULTI-DOSE
Product NDC 67979-501
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TESTOSTERONE ENANTHATE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 19531224
Marketing Category Name NDA
Labeler Name Endo Pharmaceuticals Solutions Inc
Substance Name TESTOSTERONE ENANTHATE
Strength Number 200
Strength Unit mg/mL
Pharmaceutical Classes Androgen [EPC],Androgen Receptor Agonists [MoA],Androstanes [Chemical/Ingredient]

Complete Information of DELATESTRYL


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