Pamidronate Disodium

Product NDC

0703-4075

11-digit product format

007034075

Labeler code

0703

Product ID

0703-4075_f4b7dab4-372e-480a-9d57-ff800c6e449e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pamidronate Disodium

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

Teva Parenteral Medicines, Inc.

Application

ANDA076153

Marketing category

ANDA

Marketing start

2002-04-01

Marketing end

0000-00-00

Substance

PAMIDRONATE DISODIUM

Active strength

3 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