Methylprednisolone Acetate

Product NDC

0781-3136

11-digit product format

007813136

Labeler code

0781

Product ID

0781-3136_cf85fb08-0e09-4b6b-b151-7cb8b542d31d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Methylprednisolone Acetate

Dosage form

INJECTION, SUSPENSION

Route

INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE

Labeler

Sandoz Inc

Application

ANDA040719

Marketing category

ANDA

Marketing start

2009-01-29

Marketing end

0000-00-00

Substance

METHYLPREDNISOLONE ACETATE

Active strength

40 mg/mL

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record