Progesterone

Product NDC

0093-5354

11-digit product format

000935354

Labeler code

0093

Product ID

0093-5354_f6652397-fe7e-475f-9aff-954a779ee207

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Progesterone

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

Teva Pharmaceuticals USA, Inc.

Application

ANDA202121

Marketing category

ANDA

Marketing start

2012-03-01

Marketing end

2020-05-31

Substance

PROGESTERONE

Active strength

200 mg/1

Pharmacologic classes

Progesterone [CS],Progesterone [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record