United States · FDA National Drug Code directory
Midodrine Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72603-907_142c0f69-f180-456d-930d-d332dfd3ad83
- Product NDC
- 72603-907
- Form
- TABLET
- Composition / generic term
- Midodrine Hydrochloride
- Labeler
- NorthStar RxLLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260615
- Source listing expiry
- 20271231
Source-listed ingredients
- MIDODRINE HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 BLISTER PACK in 1 CARTON (72603-907-05) / 10 TABLET in 1 BLISTER PACK (72603-907-01) · 72603-907-05
- 10 BLISTER PACK in 1 CARTON (72603-907-10) / 10 TABLET in 1 BLISTER PACK (72603-907-01) · 72603-907-10
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →