NDC 68071-3762 – Misoprostol

Misoprostol 100 ug/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3762

Product details

Brand name
Misoprostol
Generic name
Misoprostol
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076095
Marketed since
April 11, 2022
Listing expires
December 31, 2026
Pharmacologic class
Prostaglandin E1 Analog

Active ingredients

Uses, dosage, side effects and warnings for Misoprostol →

Package NDC codes (2)

Package NDCDescriptionSince
68071-3762-330 TABLET in 1 BOTTLE (68071-3762-3)Jan 10, 2025
68071-3762-990 TABLET in 1 BOTTLE (68071-3762-9)Jan 14, 2025

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