Amoxicillin

Product NDC

70518-0996

11-digit product format

705180996

Labeler code

70518

Product ID

70518-0996_8f83ccbf-5101-8466-e053-2a95a90a54f6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Amoxicillin

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA064076

Marketing category

ANDA

Marketing start

2018-01-30

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

2020-12-31

Current FDA listing

Historical FDA.report record