Procainamide Hydrochloride

Product NDC

63739-459

11-digit product format

637390459

Labeler code

63739

Product ID

63739-459_781a3972-dc50-4515-9476-42d56e1ef23d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

PROCAINAMIDE HYDROCHLORIDE

Dosage form

INJECTION, SOLUTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

McKesson Corporation

Application

ANDA089069

Marketing category

ANDA

Marketing start

2014-07-01

Marketing end

0000-00-00

Substance

PROCAINAMIDE HYDROCHLORIDE

Active strength

100 mg/mL

Pharmacologic classes

Antiarrhythmic [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record