NDC 46708-339 – Midodrine Hydrochloride

Midodrine Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC46708-339

Product details

Brand name
Midodrine Hydrochloride
Generic name
Midodrine Hydrochloride
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214734
Marketed since
January 22, 2021
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
46708-339-31100 TABLET in 1 BOTTLE (46708-339-31)Jan 22, 2021
46708-339-71500 TABLET in 1 BOTTLE (46708-339-71)Jan 22, 2021

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