Norethindrone Acetate

Product NDC

50268-602

11-digit product format

502680602

Labeler code

50268

Product ID

50268-602_7e7c28f2-97a3-660e-e053-2991aa0a1f66

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Norethindrone

Dosage form

TABLET

Route

ORAL

Labeler

AvPAK

Application

ANDA200275

Marketing category

ANDA

Marketing start

2014-11-17

Marketing end

2019-03-31

Substance

NORETHINDRONE A

Active strength

5 mg/1

Pharmacologic classes

Progesterone Co

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record