NDC 69230-318 – Omeprazole

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

Human Otc Drug

Product NDC69230-318

Product details

Brand name
Omeprazole
Generic name
Omeprazole
Labeler
Camber Consumer Care Inc
Dosage form
Tablet, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA211732
Marketed since
March 25, 2020
Listing expires
December 31, 2026
Pharmacologic class
Proton Pump Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Omeprazole →

Package NDC codes (8)

Package NDCDescriptionSince
69230-318-05500 TABLET, DELAYED RELEASE in 1 BOTTLE (69230-318-05)Oct 29, 2020
69230-318-101000 TABLET, DELAYED RELEASE in 1 BOTTLE (69230-318-10)Oct 29, 2020
69230-318-321 BLISTER PACK in 1 CARTON (69230-318-32) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACKMar 25, 2020
69230-318-332 BLISTER PACK in 1 CARTON (69230-318-33) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACKMar 25, 2020
69230-318-343 BLISTER PACK in 1 CARTON (69230-318-34) / 14 TABLET, DELAYED RELEASE in 1 BLISTER PACKMar 25, 2020
69230-318-351 BOTTLE in 1 CARTON (69230-318-35) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEMar 25, 2020
69230-318-362 BOTTLE in 1 CARTON (69230-318-36) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEMar 25, 2020
69230-318-373 BOTTLE in 1 CARTON (69230-318-37) / 14 TABLET, DELAYED RELEASE in 1 BOTTLEMar 25, 2020

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