Midodrine hydrochloride
- Product NDC
- 70771-1597
- 11-digit product format
- 707711597
- Labeler code
- 70771
- Product ID
- 70771-1597_027de750-bb64-4f6c-87ee-9c73862af579
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Midodrine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA213055
- Marketing category
- ANDA
- Marketing start
- 2020-09-17
- Substance
- MIDODRINE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 70771-1597-1 | 70771159701 | 100 TABLET in 1 BOTTLE (70771-1597-1) | 100 tablet | 2020-09-17 | No | No | Historical |