NDC 71205-905 – Midodrine Hydrochloride

Midodrine Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-905

Product details

Brand name
Midodrine Hydrochloride
Generic name
Midodrine hydrochloride
Labeler
Proficient Rx LP
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 (7)

Package NDCDescriptionSince
71205-905-00100 TABLET in 1 BOTTLE, PLASTIC (71205-905-00)Jul 20, 2021
71205-905-111000 TABLET in 1 BOTTLE, PLASTIC (71205-905-11)Jul 20, 2021
71205-905-3030 TABLET in 1 BOTTLE, PLASTIC (71205-905-30)Jul 20, 2021
71205-905-55500 TABLET in 1 BOTTLE, PLASTIC (71205-905-55)Jul 20, 2021
71205-905-6060 TABLET in 1 BOTTLE, PLASTIC (71205-905-60)Jul 20, 2021
71205-905-72120 TABLET in 1 BOTTLE, PLASTIC (71205-905-72)Jul 20, 2021
71205-905-9090 TABLET in 1 BOTTLE, PLASTIC (71205-905-90)Jul 20, 2021

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