Amoxicillin

Product NDC

70518-2078

11-digit product format

705182078

Labeler code

70518

Product ID

70518-2078_89099c08-fbd8-3c06-e053-2995a90a0331

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA065387

Marketing category

ANDA

Marketing start

2019-05-13

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

250 mg/5mL

Pharmacologic classes

Penicillin-class Antibacterial [EPC],Penicillins [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record