NDC 59762-5008 – Misoprostol

Misoprostol 200 ug/1 · Tablet · Oral

Human Prescription Drug

Product NDC59762-5008

Product details

Brand name
Misoprostol
Generic name
Misoprostol
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA019268
Marketed since
December 27, 2009
Listing expires
December 31, 2027
Pharmacologic class
Prostaglandin E1 Analog

Active ingredients

Uses, dosage, side effects and warnings for Misoprostol →

Package NDC codes (2)

Package NDCDescriptionSince
59762-5008-160 TABLET in 1 BOTTLE (59762-5008-1)Dec 27, 2009
59762-5008-2100 TABLET in 1 BOTTLE (59762-5008-2)Dec 27, 2009

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