NDC 67877-614 – Tizanidine

Tizanidine Hydrochloride 4 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC67877-614

Product details

Brand name
Tizanidine
Generic name
Tizanidine
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211798
Marketed since
January 27, 2019
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 (2)

Package NDCDescriptionSince
67877-614-05500 TABLET in 1 BOTTLE (67877-614-05)Jan 27, 2019
67877-614-15150 TABLET in 1 BOTTLE (67877-614-15)Jan 27, 2019

Recalls mentioning this NDC

Other Tizanidine products