NDC 68001-441 – Omeprazole

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

Human Otc Drug

Product NDC68001-441

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
BluePoint Laboratories
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA207740
Marketed since
June 19, 2020
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (3)

Package NDCDescriptionSince
68001-441-392 BOTTLE in 1 CARTON (68001-441-39) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)Jun 19, 2020
68001-441-403 BOTTLE in 1 CARTON (68001-441-40) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)Jun 19, 2020
68001-441-981 BOTTLE in 1 CARTON (68001-441-98) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-441-55)Jun 19, 2020

Other Omeprazole products