Prescription drug · ANDA
LOSARTAN POTASSIUM 50 mg (losartan potassium) NDC 72789-179
Losartan potassium 50 mg/1 · Tablet, Film coated · Oral · PD-Rx Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 72789-179-90 | 72789017990 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-179-90)Marketed from Mar 24, 2021 |
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)
- LOSARTAN POTASSIUM 50 mgSuffix: 50 mg
- Generic name (nonproprietary)
- losartan potassium
- Active ingredients
- Losartan potassium — 50 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090382
- Marketing start
- Listing expires
- Other FDA classes
- Angiotensin 2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 72789-179_5b8a5dd3-3e41-d1ae-e063-6294a90a0047SPL ID 5b8a5dd3-3e41-d1ae-e063-6294a90a0047
- Pharmacologic class
- Angiotensin 2 Receptor Blocker
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
N472789017990followed by a unit qualifier and the quantityPackage 72789-0179-90. 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
The FDA listing for this product does not reference a label (SPL) set.
Other NDCs under ANDA 090382
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 |
|---|---|---|---|---|
| LOSARTAN POTASSIUM 50 mglosartan potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-418 |
| LOSARTAN POTASSIUM 50 mglosartan potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 71205-598 |
| LOSARTAN POTASSIUM 25 mglosartan potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-282 |
| LOSARTAN POTASSIUM 100 mglosartan potassium | Losartan potassium 100 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals,Inc. | 68071-2203 |
| LOSARTAN POTASSIUM 25 mglosartan potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 71205-675 |
| LOSARTAN POTASSIUM 50 mglosartan potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | Strides Pharma Science Limited | 64380-934 |
| LOSARTAN POTASSIUM 25 mglosartan potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | Strides Pharma Science Limited | 64380-933 |
| LOSARTAN POTASSIUM 100 mglosartan potassium | Losartan potassium 100 mg/1 | Tablet, Film coatedOral | Strides Pharma Science Limited | 64380-935 |
| LOSARTAN POTASSIUM 50 mglosartan potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-164 |
| LOSARTAN POTASSIUM 25 mglosartan potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-163 |
| LOSARTAN POTASSIUM 100 mglosartan potassium | Losartan potassium 100 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 72789-165 |