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Ortho Micronor - 50458-194-23 - (NORETHINDRONE)

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Drug Information of Ortho Micronor

Product NDC: 50458-194
Proprietary Name: Ortho Micronor
Non Proprietary Name: NORETHINDRONE
Active Ingredient(s): .35    mg/1 & nbsp;   NORETHINDRONE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ortho Micronor

Product NDC: 50458-194
Labeler Name: Janssen Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA016954
Marketing Category: NDA
Start Marketing Date: 19730102

Package Information of Ortho Micronor

Package NDC: 50458-194-23
Package Description: 12 BLISTER PACK in 1 CARTON (50458-194-23) > 28 TABLET in 1 BLISTER PACK (50458-194-00)

NDC Information of Ortho Micronor

NDC Code 50458-194-23
Proprietary Name Ortho Micronor
Package Description 12 BLISTER PACK in 1 CARTON (50458-194-23) > 28 TABLET in 1 BLISTER PACK (50458-194-00)
Product NDC 50458-194
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name NORETHINDRONE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19730102
Marketing Category Name NDA
Labeler Name Janssen Pharmaceuticals, Inc.
Substance Name NORETHINDRONE
Strength Number .35
Strength Unit mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Ortho Micronor


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