NDC 68788-8771 – Omeprazole

Omeprazole 40 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC68788-8771

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078490
Marketed since
November 20, 2024
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8771-1100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-1)Nov 20, 2024
68788-8771-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-3)Nov 20, 2024
68788-8771-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-6)Nov 20, 2024
68788-8771-8120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-8)Nov 20, 2024
68788-8771-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8771-9)Nov 20, 2024

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