safeway acid reducer

Product NDC
21130-564
11-digit product format
211300564
Labeler code
21130
Product ID
21130-564_a2694f4b-cb2c-4efa-b138-9e5b25a78ea1
Type
HUMAN OTC DRUG
Nonproprietary name
Lansoprazole
Dosage form
CAPSULE, DELAYED RELEASE
Route
ORAL
Labeler
Safeway
Application
ANDA202319
Marketing category
ANDA
Marketing start
2022-04-18
Marketing end
0000-00-00
Substance
LANSOPRAZOLE
Active strength
15 mg/1
Pharmacologic classes
Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21130-564SAFEWAY ACID REDUCER (LANSOPRAZOLE) CAPSULE, DELAYED RELEASE [SAFEWAY]4Legacy NDC20250514_5fd96bb9-bf1e-4acc-aa86-a303a3497612.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
21130-564-01211300564011 BOTTLE in 1 CARTON (21130-564-01) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE1 bottle2022-04-180000-00-00NoNoCurrent
21130-564-03211300564033 BOTTLE in 1 CARTON (21130-564-03) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE3 bottle2022-04-180000-00-00NoNoCurrent