Amoxicillin

Product NDC
76420-871
11-digit product format
764200871
Labeler code
76420
Product ID
76420-871_26377eb9-ab0a-505d-e063-6394a90af5db
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
CAPSULE
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA065271
Marketing category
ANDA
Marketing start
2017-12-12
Substance
AMOXICILLIN
Active strength
500 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
76420-871-037642008710321 CAPSULE in 1 BOTTLE, PLASTIC (76420-871-03) 21 capsule2024-11-06NoNoHistorical
76420-871-057642008710530 CAPSULE in 1 BLISTER PACK (76420-871-05) 30 capsule2024-11-06NoNoHistorical
76420-871-067642008710621 CAPSULE in 1 BLISTER PACK (76420-871-06) 21 capsule2024-11-06NoNoHistorical
76420-871-077642008710728 CAPSULE in 1 BLISTER PACK (76420-871-07) 28 capsule2024-11-06NoNoHistorical
76420-871-087642008710830 CAPSULE in 1 BOTTLE, PLASTIC (76420-871-08) 30 capsule2024-11-06NoNoHistorical
76420-871-097642008710920 CAPSULE in 1 BOTTLE, PLASTIC (76420-871-09) 20 capsule2024-11-06NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AmoxicillinAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2024-11-05HUMAN PRESCRIPTION DRUG LABEL1