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Progesterone - 0093-5353-01 - (Progesterone)

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Drug Information of Progesterone

Product NDC: 0093-5353
Proprietary Name: Progesterone
Non Proprietary Name: Progesterone
Active Ingredient(s): 100    mg/1 & nbsp;   Progesterone
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Progesterone

Product NDC: 0093-5353
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202121
Marketing Category: ANDA
Start Marketing Date: 20120301

Package Information of Progesterone

Package NDC: 0093-5353-01
Package Description: 100 CAPSULE in 1 BOTTLE (0093-5353-01)

NDC Information of Progesterone

NDC Code 0093-5353-01
Proprietary Name Progesterone
Package Description 100 CAPSULE in 1 BOTTLE (0093-5353-01)
Product NDC 0093-5353
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Progesterone
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120301
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name PROGESTERONE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Progesterone [Chemical/Ingredient],Progesterone [EPC]

Complete Information of Progesterone


General Information