NDC 0713-0135 – Prochlorperazine

Prochlorperazine 25 mg/1 · Suppository · Rectal

Human Prescription Drug

Product NDC0713-0135

Product details

Brand name
Prochlorperazine
Generic name
Prochlorperazine
Labeler
Cosette Pharmaceuticals, Inc.
Dosage form
Suppository
Route
Rectal
Marketing category
ANDA · ANDA040058
Marketed since
November 30, 1993
Listing expires
December 31, 2026
Pharmacologic class
Phenothiazine

Active ingredients

Uses, dosage, side effects and warnings for Prochlorperazine →

Package NDC codes (2)

Package NDCDescriptionSince
0713-0135-101000 BLISTER PACK in 1 CARTON (0713-0135-10) / 1 SUPPOSITORY in 1 BLISTER PACKNov 30, 1993
0713-0135-1212 BLISTER PACK in 1 CARTON (0713-0135-12) / 1 SUPPOSITORY in 1 BLISTER PACKNov 30, 1993

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