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Follistim AQ - 0052-0316-01 - (follitropin)

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Drug Information of Follistim AQ

Product NDC: 0052-0316
Proprietary Name: Follistim AQ
Non Proprietary Name: follitropin
Active Ingredient(s): 650    [iU]/.78mL & nbsp;   follitropin
Administration Route(s): SUBCUTANEOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Follistim AQ

Product NDC: 0052-0316
Labeler Name: Organon USA Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021211
Marketing Category: NDA
Start Marketing Date: 20100628

Package Information of Follistim AQ

Package NDC: 0052-0316-01
Package Description: 1 KIT in 1 CARTON (0052-0316-01) > 1 CARTRIDGE in 1 KIT > .78 mL in 1 CARTRIDGE

NDC Information of Follistim AQ

NDC Code 0052-0316-01
Proprietary Name Follistim AQ
Package Description 1 KIT in 1 CARTON (0052-0316-01) > 1 CARTRIDGE in 1 KIT > .78 mL in 1 CARTRIDGE
Product NDC 0052-0316
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name follitropin
Dosage Form Name INJECTION, SOLUTION
Route Name SUBCUTANEOUS
Start Marketing Date 20100628
Marketing Category Name NDA
Labeler Name Organon USA Inc.
Substance Name FOLLITROPIN
Strength Number 650
Strength Unit [iU]/.78mL
Pharmaceutical Classes Gonadotropin [EPC],Gonadotropins [Chemical/Ingredient]

Complete Information of Follistim AQ


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