Prochlorperazine

Product NDC

68071-3259

11-digit product format

680713259

Labeler code

68071

Product ID

68071-3259_50217b0f-a6e4-6c82-e054-00144ff88e88

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Prochlorperazine

Dosage form

SUPPOSITORY

Route

RECTAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA040058

Marketing category

ANDA

Marketing start

1993-11-30

Marketing end

0000-00-00

Substance

PROCHLORPERAZINE

Active strength

25 mg/1

Pharmacologic classes

Phenothiazine [EPC],Phenothiazines [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record