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Norethindrone Acetate - 0555-0211-10 - (Norethindrone Acetate)

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Drug Information of Norethindrone Acetate

Product NDC: 0555-0211
Proprietary Name: Norethindrone Acetate
Non Proprietary Name: Norethindrone Acetate
Active Ingredient(s): 5    mg/1 & nbsp;   Norethindrone Acetate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Norethindrone Acetate

Product NDC: 0555-0211
Labeler Name: Barr Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075951
Marketing Category: ANDA
Start Marketing Date: 20010629

Package Information of Norethindrone Acetate

Package NDC: 0555-0211-10
Package Description: 50 TABLET in 1 BOTTLE (0555-0211-10)

NDC Information of Norethindrone Acetate

NDC Code 0555-0211-10
Proprietary Name Norethindrone Acetate
Package Description 50 TABLET in 1 BOTTLE (0555-0211-10)
Product NDC 0555-0211
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Norethindrone Acetate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20010629
Marketing Category Name ANDA
Labeler Name Barr Laboratories 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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