NDC 23155-971 – Midodrine Hydrochloride

Midodrine Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-971

Product details

Brand name
Midodrine Hydrochloride
Generic name
Midodrine hydrochloride
Labeler
Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076725
Marketed since
March 25, 2026
Listing expires
December 31, 2027
Pharmacologic class
alpha-Adrenergic Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
23155-971-01100 TABLET in 1 BOTTLE (23155-971-01)Mar 25, 2026

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