Misoprostol

Product NDC

0179-0218

11-digit product format

001790218

Labeler code

0179

Product ID

0179-0218_7be9daee-61ad-9a81-e053-2a91aa0a5247

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Misoprostol

Dosage form

TABLET

Route

ORAL

Labeler

KAISER FOUNDATION HOSPITALS

Application

ANDA091667

Marketing category

ANDA

Marketing start

2016-09-20

Marketing end

2019-12-31

Substance

MISOPROSTOL

Active strength

200 ug/1

Pharmacologic classes

Prostaglandin E1 Analog [EPC],Prostaglandins E, Synthetic [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record