Sandostatin

Product NDC

0078-0184

11-digit product format

000780184

Labeler code

0078

Product ID

0078-0184_70137f2b-5951-4762-a04a-a002cfac8b87

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

octreotide acetate

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS; SUBCUTANEOUS

Labeler

Novartis Pharmaceuticals Corporation

Application

NDA019667

Marketing category

NDA

Marketing start

1988-10-21

Marketing end

0000-00-00

Substance

OCTREOTIDE ACETATE

Active strength

1000 ug/mL

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record