Norethindrone

Product NDC

50090-2150

11-digit product format

500902150

Labeler code

50090

Product ID

50090-2150_3037dd29-c035-4950-a420-3f0d49c8a9c1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Norethindrone

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA091209

Marketing category

ANDA

Marketing start

2010-11-03

Marketing end

0000-00-00

Substance

NORETHINDRONE

Active strength

0 mg/1

Pharmacologic classes

Progesterone Congeners [CS],Progestin [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record