NDC 71335-1705 – Midodrine Hydrochloride

Midodrine Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1705

Product details

Brand name
Midodrine Hydrochloride
Generic name
Midodrine Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207613
Marketed since
April 1, 2019
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
71335-1705-130 TABLET in 1 BOTTLE (71335-1705-1)Sep 10, 2020

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