NDC 0121-0581 – Haloperidol

Haloperidol 2 mg/mL · Solution · Oral

Human Prescription Drug

Product NDC0121-0581

Product details

Brand name
Haloperidol
Generic name
Haloperidol
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
Solution
Route
Oral
Marketing category
ANDA · ANDA073037
Marketed since
November 10, 2009
Listing expires
December 31, 2026
Pharmacologic class
Typical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Haloperidol →

Package NDC codes (3)

Package NDCDescriptionSince
0121-0581-04120 mL in 1 BOTTLE (0121-0581-04)Nov 10, 2009
0121-0581-0510 TRAY in 1 CASE (0121-0581-05) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSENov 10, 2009
0121-0581-1515 mL in 1 BOTTLE (0121-0581-15)Jun 12, 2020

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