NDC 0904-6818 – Midodrine Hydrochloride

Midodrine Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC0904-6818

Product details

Brand name
Midodrine Hydrochloride
Generic name
Midodrine Hydrochloride
Labeler
Major Pharmaceuticals
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077746
Marketed since
September 12, 2006
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Midodrine Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
0904-6818-0650 BLISTER PACK in 1 CARTON (0904-6818-06) / 1 TABLET in 1 BLISTER PACKSep 12, 2006
0904-6818-61100 BLISTER PACK in 1 CARTON (0904-6818-61) / 1 TABLET in 1 BLISTER PACKSep 12, 2006

Recalls mentioning this NDC

Other Midodrine Hydrochloride products