PROGESTERONE

Product NDC

42291-690

11-digit product format

422910690

Labeler code

42291

Product ID

42291-690_7b0b6976-3aa2-02f6-e053-2a91aa0afea6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

PROGESTERONE

Dosage form

CAPSULE

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA200900

Marketing category

ANDA

Marketing start

2014-09-29

Marketing end

0000-00-00

Substance

PROGESTERONE

Active strength

100 mg/1

Pharmacologic classes

Progesterone [CS],Progesterone [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record