Prescription drug · ANDA
Losartan Potassium NDC 70518-3282
Losartan potassium 50 mg/1 · Tablet · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-3282-0 | 70518328200 | 60 TABLET in 1 BLISTER PACK (70518-3282-0)Marketed from Dec 6, 2021 | |
| 70518-3282-1 | 70518328201 | 30 TABLET in 1 BLISTER PACK (70518-3282-1)Marketed from Dec 17, 2021 | |
| 70518-3282-3 | 70518328203 | 100 TABLET in 1 BOTTLE, PLASTIC (70518-3282-3)Marketed from Sep 17, 2026 |
How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
- Generic name (nonproprietary)
- losartan potassium
- Active ingredients
- Losartan potassium — 50 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- REMEDYREPACK INC.
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 078232
- Marketing start
- Listing expires
- Other FDA classes
- Angiotensin 2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 70518-3282_5bacf1c2-9eb6-6eca-e063-6394a90a2950SPL ID 5bacf1c2-9eb6-6eca-e063-6394a90a2950
- 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
N470518328200followed by a unit qualifier and the quantityPackage 70518-3282-00. 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 078232
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 | Losartan potassium 50 mg/1 | TabletOral | A-S Medication Solutions | 50090-5480 |
| Losartan Potassium | Losartan potassium 100 mg/1 | TabletOral | A-S Medication Solutions | 50090-3403 |
| Losartan Potassium | Losartan potassium 25 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-210 |
| Losartan Potassium | Losartan potassium 50 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-211 |
| Losartan Potassium | Losartan potassium 100 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-212 |
| Losartan Potassium | Losartan potassium 25 mg/1 | TabletOral | A-S Medication Solutions | 50090-5626 |
| Losartan Potassium | Losartan potassium 25 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-307 |
| Losartan Potassium | Losartan potassium 50 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-308 |
| Losartan Potassium | Losartan potassium 100 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-309 |
| Losartan Potassium | Losartan potassium 25 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-376 |
| Losartan Potassium | Losartan potassium 50 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-377 |
| Losartan Potassium | Losartan potassium 100 mg/1 | TabletOral | Lupin Pharmaceuticals, Inc. | 68180-378 |