Pamidronate Disodium

Product NDC

63323-735

11-digit product format

633230735

Labeler code

63323

Product ID

63323-735_7d3a4a7d-7ed2-af9a-e053-2991aa0a708f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

PAMIDRONATE DISODIUM

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Fresenius Kabi USA, LLC

Application

ANDA076207

Marketing category

ANDA

Marketing start

2002-05-19

Marketing end

0000-00-00

Substance

PAMIDRONATE DISODIUM

Active strength

9 mg/mL

Pharmacologic classes

Bisphosphonate [EPC],Diphosphonates [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record