NDC 70700-159 – Midodrine Hydrochloride

Midodrine Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70700-159

Product details

Brand name
Midodrine Hydrochloride
Generic name
Midodrine hydrochloride
Labeler
Xiromed, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207849
Marketed since
October 15, 2020
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
70700-159-01100 TABLET in 1 BOTTLE, PLASTIC (70700-159-01)Oct 15, 2020

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