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Progesterone - 17478-767-10 - (Progesterone)

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Drug Information of Progesterone

Product NDC: 17478-767
Proprietary Name: Progesterone
Non Proprietary Name: Progesterone
Active Ingredient(s): 200    mg/1 & nbsp;   Progesterone
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Progesterone

Product NDC: 17478-767
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200456
Marketing Category: ANDA
Start Marketing Date: 20121004

Package Information of Progesterone

Package NDC: 17478-767-10
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (17478-767-10)

NDC Information of Progesterone

NDC Code 17478-767-10
Proprietary Name Progesterone
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (17478-767-10)
Product NDC 17478-767
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Progesterone
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20121004
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name PROGESTERONE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Progesterone [Chemical/Ingredient],Progesterone [EPC]

Complete Information of Progesterone


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