Midodrine Hydrochloride
- Product NDC
- 55154-8086
- 11-digit product format
- 551548086
- Labeler code
- 55154
- Product ID
- 55154-8086_56df3d55-68c0-44ef-ae77-26b7abfa7811
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA077746
- Marketing category
- ANDA
- Marketing start
- 2006-09-12
- 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 |
|---|
| 55154-8086-0 | 55154808600 | 10 BLISTER PACK in 1 BAG (55154-8086-0) / 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2006-09-12 | No | No | Historical |