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Norethindrone Acetate - 42291-650-90 - (Norethindrone)

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Drug Information of Norethindrone Acetate

Product NDC: 42291-650
Proprietary Name: Norethindrone Acetate
Non Proprietary Name: Norethindrone
Active Ingredient(s): 5    mg/1 & nbsp;   Norethindrone
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Norethindrone Acetate

Product NDC: 42291-650
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200275
Marketing Category: ANDA
Start Marketing Date: 20130618

Package Information of Norethindrone Acetate

Package NDC: 42291-650-90
Package Description: 90 TABLET in 1 BOTTLE (42291-650-90)

NDC Information of Norethindrone Acetate

NDC Code 42291-650-90
Proprietary Name Norethindrone Acetate
Package Description 90 TABLET in 1 BOTTLE (42291-650-90)
Product NDC 42291-650
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norethindrone
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130618
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
Substance Name NORETHINDRONE ACETATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Progesterone Congeners [Chemical/Ingredient],Progestin [EPC]

Complete Information of Norethindrone Acetate


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