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
- 0245-0211_18b0b9f5-6026-479e-af12-92b0e71a9d6b
- Product NDC
- 0245-0211
- Form
- TABLET
- Composition / generic term
- midodrine hydrochloride
- Labeler
- Upsher-Smith laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20041103
- Source listing expiry
- 20261231
Source-listed ingredients
- MIDODRINE HYDROCHLORIDE — 2.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 BLISTER PACK in 1 CARTON (0245-0211-01) / 1 TABLET in 1 BLISTER PACK (0245-0211-89) · 0245-0211-01
- 100 TABLET in 1 BOTTLE (0245-0211-11) · 0245-0211-11
Source and coverage
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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.
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