Cephalexin

Product NDC

68071-4177

11-digit product format

680714177

Labeler code

68071

Product ID

68071-4177_5fc4ab7e-cee6-30d7-e053-2a91aa0ae81b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Cephalexin

Dosage form

POWDER, FOR SUSPENSION

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA062703

Marketing category

ANDA

Marketing start

1990-09-30

Marketing end

0000-00-00

Substance

CEPHALEXIN

Active strength

250 mg/5mL

Pharmacologic classes

Cephalosporin Antibacterial [EPC],Cephalosporins [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record