Amoxicillin

Product NDC
76420-832
11-digit product format
764200832
Labeler code
76420
Product ID
76420-832_1f9dd2b3-12f6-c5c3-e063-6294a90a8065
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
CAPSULE
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA065271
Marketing category
ANDA
Marketing start
2005-11-09
Substance
AMOXICILLIN
Active strength
250 mg/1
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
76420-832-0176420083201100 CAPSULE in 1 BOTTLE (76420-832-01) 100 capsule2024-08-14NoNoHistorical
76420-832-0576420083205500 CAPSULE in 1 BOTTLE (76420-832-05) 500 capsule2024-08-14NoNoHistorical
76420-832-207642008322020 CAPSULE in 1 BOTTLE (76420-832-20) 20 capsule2024-08-14NoNoHistorical
76420-832-307642008323030 CAPSULE in 1 BOTTLE (76420-832-30) 30 capsule2024-08-14NoNoHistorical
76420-832-507642008325050 CAPSULE in 1 BOTTLE (76420-832-50) 50 capsule2024-08-14NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AmoxicillinAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2024-08-14HUMAN PRESCRIPTION DRUG LABEL1