Cefadroxil

Product NDC

70518-2271

11-digit product format

705182271

Labeler code

70518

Product ID

70518-2271_9121b464-d0e2-0a04-e053-2a95a90ad9ae

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefadroxil

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA065352

Marketing category

ANDA

Marketing start

2019-08-19

Marketing end

0000-00-00

Substance

CEFADROXIL

Active strength

500 mg/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record