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Product NDC
24385-201
11-digit product format
243850201
Labeler code
24385
Product ID
24385-201_fdf66de5-7d61-4908-ac96-7625c575dbe8
Type
HUMAN OTC DRUG
Nonproprietary name
famotidine, calcium carbonate and magnesium hydroxide
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
Amerisource Bergen
Application
ANDA077355
Marketing category
ANDA
Marketing start
2008-08-04
Marketing end
0000-00-00
Substance
FAMOTIDINE; MAGNESIUM HYDROXIDE; CALCIUM CARBONATE
Active strength
10 mg/1; mg/1; mg/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
24385-201-58EA - Each24385-201bba6a24f-bdcc-4028-ab66-9458fd076c6212012-07-24
24385-201-63EA - Each24385-201d00b65e2-e907-430e-bdd0-36e9b2cac09d12012-07-24