Midodrine Hydrochloride
- Product NDC
- 48433-075
- 11-digit product format
- 484330075
- Labeler code
- 48433
- Product ID
- 48433-075_4d6888fa-c1ed-370b-e063-6394a90a59c2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- midodrine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Safecor Health LLC
- Application
- ANDA076577
- Marketing category
- ANDA
- Marketing start
- 2026-03-13
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Midodrine Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MIDODRINE HYDROCHLORIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 59JV96YTXV |
| Rxcui | 993470 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 48433-075-01 | Midodrine Hydrochloride | 1 in 1 BLISTER PACK | TABLET | 1 | | 3 |
| 48433-075-20 | Midodrine Hydrochloride | 100 in 1 CARTON | TABLET | 100 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 48433-075-01 | 48433007501 | 1 in 1 BLISTER PACK | | | | | Historical |
| 48433-075-20 | 48433007520 | 100 BLISTER PACK in 1 CARTON (48433-075-20) / 1 TABLET in 1 BLISTER PACK (48433-075-01) | 100 blister pack | 2026-03-13 | No | No | Current |