Prochlorperazine Edisylate

Product NDC

0641-0491

11-digit product format

006410491

Labeler code

0641

Product ID

0641-0491_7b251584-d98e-459b-9a71-8574bd5733d1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prochlorperazine Edisylate

Dosage form

INJECTION

Route

INTRAMUSCULAR; INTRAVENOUS

Labeler

Baxter Healthcare Corporation

Application

ANDA089903

Marketing category

ANDA

Marketing start

2011-01-14

Marketing end

0000-00-00

Substance

PROCHLORPERAZINE EDISYLATE

Active strength

5 mg/mL

Pharmacologic classes

Phenothiazine [EPC],Phenothiazines [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record