Octreotide Acetate

Product NDC

0781-3165

11-digit product format

007813165

Labeler code

0781

Product ID

0781-3165_b02b276f-9007-4ec7-8bcd-40f14213d7f5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Octreotide Acetate

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS; SUBCUTANEOUS

Labeler

Sandoz Inc

Application

NDA019667

Marketing category

NDA

Marketing start

1988-10-21

Marketing end

0000-00-00

Substance

OCTREOTIDE ACETATE

Active strength

200 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