Amoxicillin

Product NDC
70518-3832
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Amoxicillin
Dosage form
CAPSULE
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA065271
Marketing category
ANDA
Substance
AMOXICILLIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
70518-3832-114 CAPSULE in 1 BOTTLE, PLASTIC (70518-3832-1) 2025-01-20NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
AmoxicillinREMEDYREPACK INC.2025-09-22HUMAN PRESCRIPTION DRUG LABEL6