NDC 85509-1180 – Tizanidine

Tizanidine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC85509-1180

Product details

Brand name
Tizanidine
Generic name
Tizanidine
Labeler
PHOENIX RX LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076286
Marketed since
July 3, 2002
Listing expires
December 31, 2026
Pharmacologic class
Central alpha-2 Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Tizanidine →

Package NDC codes (5)

Package NDCDescriptionSince
85509-1180-1120 TABLET in 1 BOTTLE (85509-1180-1)Jul 31, 2025
85509-1180-228 TABLET in 1 BOTTLE (85509-1180-2)Jul 31, 2025
85509-1180-330 TABLET in 1 BOTTLE (85509-1180-3)Jul 31, 2025
85509-1180-660 TABLET in 1 BOTTLE (85509-1180-6)Jul 31, 2025
85509-1180-990 TABLET in 1 BOTTLE (85509-1180-9)Jul 31, 2025

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