Prescription drug · ANDA
Midodrine Hydrochloride NDC 72603-605
Midodrine hydrochloride 2.5 mg/1 · Tablet · Oral · NorthStar Rx LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72603-605-01 | 72603060501 | 100 TABLET in 1 BOTTLE (72603-605-01)Marketed from Apr 21, 2025 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Midodrine Hydrochloride
- Generic name (nonproprietary)
- midodrine hydrochloride
- Active ingredients
- Midodrine hydrochloride — 2.5 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- NorthStar Rx LLC
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 212543
- Marketing start
- Listing expires
- Other FDA classes
- Adrenergic alpha-Agonists (Mechanism)
- Identifiers
- Product ID 72603-605_3370f087-6bac-2032-e063-6394a90a9a60SPL ID 3370f087-6bac-2032-e063-6394a90a9a60SPL set ID b015c98f-57e6-410b-9c9d-8898aa22082aRxCUI 993462, 993466, 993470UNII 59JV96YTXVUPC 0372603606010, 0372603605013, 0372603607017
- Pharmacologic class
- alpha-Adrenergic Agonist
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N472603060501followed by a unit qualifier and the quantityPackage 72603-0605-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 212543
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Midodrine Hydrochloride | Midodrine hydrochloride 5 mg/1 | TabletOral | Bryant Ranch Prepack | 71335-2171 |
| Midodrine Hydrochloride | Midodrine hydrochloride 2.5 mg/1 | TabletOral | TruPharma, LLC | 52817-323 |
| Midodrine Hydrochloride | Midodrine hydrochloride 5 mg/1 | TabletOral | TruPharma, LLC | 52817-324 |
| Midodrine Hydrochloride | Midodrine hydrochloride 10 mg/1 | TabletOral | TruPharma, LLC | 52817-325 |
| Midodrine Hydrochloride | Midodrine hydrochloride 2.5 mg/1 | TabletOral | Advagen Pharma Limited | 72888-112 |
| Midodrine Hydrochloride | Midodrine hydrochloride 5 mg/1 | TabletOral | Advagen Pharma Limited | 72888-113 |
| Midodrine Hydrochloride | Midodrine hydrochloride 10 mg/1 | TabletOral | Advagen Pharma Limited | 72888-114 |
| Midodrine Hydrochloride | Midodrine hydrochloride 5 mg/1 | TabletOral | NorthStar Rx LLC | 72603-606 |
| Midodrine Hydrochloride | Midodrine hydrochloride 10 mg/1 | TabletOral | NorthStar Rx LLC | 72603-607 |
| Midodrine Hydrochloride | Midodrine hydrochloride 5 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 72789-468 |
| Midodrine Hydrochloride | Midodrine hydrochloride 2.5 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 72789-465 |
| Midodrine Hydrochloride | Midodrine hydrochloride 10 mg/1 | TabletOral | PD-Rx Pharmaceuticals, Inc. | 72789-467 |