Pralidoxime Chloride

Product NDC

11704-251

11-digit product format

117040251

Labeler code

11704

Product ID

11704-251_c7e5b5e2-5de7-4b70-89d8-92fc6c0d7c40

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Pralidoxime Chloride

Dosage form

INJECTION

Route

INTRAMUSCULAR

Labeler

Meridian Medical Technologies, Inc.

Application

NDA018986

Marketing category

NDA

Marketing start

1983-04-26

Marketing end

0000-00-00

Substance

PRALIDOXIME CHLORIDE

Active strength

600 mg/2mL

Pharmacologic classes

Cholinesterase Reactivator [EPC],Cholinesterase Reactivators [MoA]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record