Amoxicillin

Product NDC

70518-1099

11-digit product format

705181099

Labeler code

70518

Product ID

70518-1099_69acc713-8ff1-6868-e053-2a91aa0aa00c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA062058

Marketing category

ANDA

Marketing start

2018-04-06

Marketing end

0000-00-00

Substance

AMOXICILLIN

Active strength

500 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record