Midodrine Hydrochloride
- Product NDC
- 72162-2561
- 11-digit product format
- 721622561
- Labeler code
- 72162
- Product ID
- 72162-2561_65c0ebb0-f578-4021-a11b-163e473c5092
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212774
- Marketing category
- ANDA
- Marketing start
- 2020-08-10
- Substance
- MIDODRINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 59JV96YTXV | MIDODRINE HYDROCHLORIDE | 43218-56-0 | MIDODRINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2561-1 | 72162256101 | 100 TABLET in 1 BOTTLE (72162-2561-1) | 100 tablet | 2025-11-04 | No | No | Historical |