Amoxicillin

Product NDC
49999-168
11-digit product format
499990168
Labeler code
49999
Product ID
49999-168_387f4ae6-d12a-48a0-b87c-52d7f10925e4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA065387
Marketing category
ANDA
Marketing start
2007-03-26
Marketing end
0000-00-00
Substance
AMOXICILLIN
Active strength
250 mg/5mL
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