Prednisone

Product NDC

68071-4546

11-digit product format

680714546

Labeler code

68071

Product ID

68071-4546_74c01b06-ea40-7d7b-e053-2a91aa0a96e7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prednisone

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA080356

Marketing category

ANDA

Marketing start

1990-01-01

Marketing end

0000-00-00

Substance

PREDNISONE

Active strength

5 mg/1

Pharmacologic classes

Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record