Cefaclor

Product NDC

16571-070

11-digit product format

165710070

Labeler code

16571

Product ID

16571-070_309bc345-79d1-4e7a-80fc-cfafd8e1010b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cefaclor

Dosage form

SUSPENSION

Route

ORAL

Labeler

Pack Pharmaceuticals, LLC

Application

ANDA065412

Marketing category

ANDA

Marketing start

2012-10-25

Marketing end

0000-00-00

Substance

CEFACLOR

Active strength

125 mg/5mL

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record