Polymyxin B

Product NDC

51991-939

11-digit product format

519910939

Labeler code

51991

Product ID

51991-939_0043d5d0-4e8e-4ad4-9e1a-eedfa4da66fa

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Polymyxin B

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC

Labeler

Breckenridge Pharmaceutic

Application

ANDA207322

Marketing category

ANDA

Marketing start

2016-06-01

Marketing end

2019-03-31

Substance

POLYMYXIN B SUL

Active strength

500000 1/1

Pharmacologic classes

Polymyxin-class

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record