Nortrel

Product NDC
50090-3229
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Norethindrone and Ethinyl Estradiol
Dosage form
KIT
Labeler
A-S Medication Solutions
Application
ANDA072695
Marketing category
ANDA
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-3229-01 KIT in 1 KIT (50090-3229-0) 2017-10-30NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Nortrel ® (norethindrone and ethinyl estradiol tablets USP)A-S Medication Solutions2024-05-07HUMAN PRESCRIPTION DRUG LABEL11