Octreotide Acetate

Product NDC

0781-3166

11-digit product format

007813166

Labeler code

0781

Product ID

0781-3166_4e5348ae-d032-4eea-babc-2cc54c66616e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Octreotide Acetate

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS; SUBCUTANEOUS

Labeler

Sandoz Inc

Application

NDA019667

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-02-04

Marketing end

0000-00-00

Substance

OCTREOTIDE ACETATE

Active strength

50 ug/mL

Pharmacologic classes

Somatostatin Analog [EPC],Somatostatin Receptor Agonists [MoA]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record