Amoxicillin

Product NDC
33261-488
11-digit product format
332610488
Labeler code
33261
Product ID
33261-488_9abd651c-3fc9-4426-9392-6e2a783d3d8e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Aidarex Pharmaceuticals LLC
Application
ANDA065256
Marketing category
ANDA
Marketing start
2005-11-09
Marketing end
0000-00-00
Substance
AMOXICILLIN
Active strength
875 mg/1
Pharmacologic classes
Penicillin-class Antibacterial [EPC],Penicillins [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
804826J2HUAMOXICILLIN61336-70-7AMOXICILLIN

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Amoxicillin - Aidarex Pharmaceuticals LLCAidarex Pharmaceuticals LLC2013-11-22HUMAN PRESCRIPTION DRUG LABEL1