NDC 72789-482 – Omeprazole

Omeprazole 20 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC72789-482

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA078490
Marketed since
March 1, 2014
Listing expires
December 31, 2027
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (4)

Package NDCDescriptionSince
72789-482-1414 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-14)May 7, 2025
72789-482-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-30)Jan 25, 2025
72789-482-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-60)Mar 20, 2025
72789-482-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-482-90)Jan 23, 2025

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