NDC 0185-0022 – Orphenadrine Citrate

Orphenadrine Citrate 100 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug 2 recalls

Product NDC0185-0022

Product details

Brand name
Orphenadrine Citrate
Generic name
Orphenadrine Citrate
Labeler
Sandoz Inc
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA040327
Marketed since
February 15, 2000
Marketing end
March 20, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Orphenadrine citrate →

Package NDC codes (1)

Package NDCDescriptionSince
0185-0022-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0185-0022-01)Feb 15, 2000

Recalls mentioning this NDC

Other Orphenadrine citrate products