Amoxicillin

Product NDC
76420-833
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
CAPSULE
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA065271
Marketing category
ANDA
Substance
AMOXICILLIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
76420-833-01100 CAPSULE in 1 BOTTLE (76420-833-01) 2024-08-14NoHistorical
76420-833-05500 CAPSULE in 1 BOTTLE (76420-833-05) 2024-08-14NoHistorical
76420-833-2020 CAPSULE in 1 BOTTLE (76420-833-20) 2024-08-14NoHistorical
76420-833-3030 CAPSULE in 1 BOTTLE (76420-833-30) 2024-08-14NoHistorical
76420-833-5050 CAPSULE in 1 BOTTLE (76420-833-50) 2024-08-14NoHistorical

Related DailyMed Labels

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