ShopRite Dual Action Complete

Product NDC
41190-003
11-digit product format
411900003
Labeler code
41190
Product ID
41190-003_f9dca354-1a72-4d40-b2c5-5727eabba5a9
Type
HUMAN OTC DRUG
Nonproprietary name
famotidine, calcium carbonate and magnesium hydroxide
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
Wakefern Food Corporation
Application
ANDA077355
Marketing category
ANDA
Marketing start
2016-02-05
Marketing end
0000-00-00
Substance
FAMOTIDINE; MAGNESIUM HYDROXIDE; CALCIUM CARBONATE
Active strength
10 mg/1; mg/1; mg/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41190-003-632021-10-06C16284748780-19d75b9d0-b6fe-f424-e053-dadaa90a57cef9dca354-1a72-4d40-b2c5-5727eabba5a9
41190-003-632020-01-31C16284748780-19d75b9d0-b6fe-f424-e053-dadaa90a57cef9dca354-1a72-4d40-b2c5-5727eabba5a9