NDC 68382-081 – Haloperidol

Haloperidol 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-081

Product details

Brand name
Haloperidol
Generic name
Haloperidol
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077580
Marketed since
January 3, 2008
Listing expires
December 31, 2026
Pharmacologic class
Typical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Haloperidol →

Package NDC codes (2)

Package NDCDescriptionSince
68382-081-01100 TABLET in 1 BOTTLE (68382-081-01)Jan 3, 2008
68382-081-0630 TABLET in 1 BOTTLE (68382-081-06)Jan 3, 2008

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