Amoxicillin

Product NDC
76420-573
11-digit product format
764200573
Labeler code
76420
Product ID
76420-573_fe4d14a5-07d5-9345-e053-6294a90a78b2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA061931
Marketing category
ANDA
Marketing start
1990-09-30
Substance
AMOXICILLIN
Active strength
250 mg/5mL
Pharmacologic classes
Penicillin-class Antibacterial [EPC], Penicillins [CS]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
804826J2HUAMOXICILLIN61336-70-7AMOXICILLIN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
76420-573-1076420057310100 mL in 1 BOTTLE (76420-573-10) 100 ml2023-06-17NoNoHistorical
76420-573-1576420057315150 mL in 1 BOTTLE (76420-573-15) 150 ml2023-06-17NoNoHistorical
76420-573-807642005738080 mL in 1 BOTTLE (76420-573-80) 80 ml2023-06-17NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AmoxicillinAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2023-06-17HUMAN PRESCRIPTION DRUG LABEL1