NDC 68382-737 – Midodrine hydrochloride

Midodrine Hydrochloride 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-737

Product details

Brand name
Midodrine hydrochloride
Generic name
Midodrine hydrochloride
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213055
Marketed since
September 17, 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
68382-737-01100 TABLET in 1 BOTTLE (68382-737-01)Sep 17, 2020

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