Prescription drug · ANDA
Losartan Potassium (Losartan) NDC 62207-742
Losartan potassium 50 mg/1 · Tablet · Oral · Granules India Ltd
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 62207-742-49 | 6220707424962207074249 | 1000 TABLET in 1 BOTTLE (62207-742-49)Marketed from Mar 18, 2025 | |
| 62207-742-54 | 6220707425462207074254 | 30 TABLET in 1 BOTTLE (62207-742-54)Marketed from Mar 18, 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)
- Losartan Potassium
- Generic name (nonproprietary)
- losartan
- Active ingredients
- Losartan potassium — 50 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- Granules India LtdNDC labeler code 62207
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 215959
- Marketing start
- Listing expires
- Other FDA classes
- Angiotensin 2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 62207-742_5d3e8077-9505-b597-e063-6294a90ad11dSPL ID 5d3e8077-9505-b597-e063-6294a90ad11d
- 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
N462207074249followed by a unit qualifier and the quantityPackage 62207-0742-49. 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.
About NDC 62207-742
- What is NDC 62207-742?
- 62207-742 is the product NDC for Losartan Potassium (losartan), Losartan potassium 50 mg/1 tablet, listed with the FDA by Granules India Ltd. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Losartan Potassium (Losartan).
- What is the active ingredient?
- Losartan potassium.
- Who is the labeler?
- Granules India Ltd, NDC labeler code 62207. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Losartan Potassium?
- 173 other product NDCs are listed under this name. See all Losartan Potassium NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Losartan Potassium products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Losartan potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | St. Mary's Medical Park Pharmacy | 60760-876 | 60760-0876-30 |
| Losartan potassium | Losartan potassium 100 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4773 | 70518-4773-00 |
| Losartan Potassiumlosartan | Losartan potassium 50 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-4160 | 68788-4160-0368788-4160-09 |
| Losartan Potassium | Losartan potassium 100 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4695 | 70518-4695-0070518-4695-01 |
| Losartan Potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | Unit Dose Solutions, Inc. | 87441-052 | 87441-0052-01 |
| Losartan Potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | Unit Dose Solutions, Inc. | 87441-053 | 87441-0053-01 |
| Losartan Potassium | Losartan potassium 100 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-0702 | 67046-0702-03 |
| Losartan potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-4127 | 68788-4127-0368788-4127-09 |
| Losartan Potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1088 | 67046-1088-03 |
| Losartan potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-4091 | 68788-4091-0368788-4091-09 |
Other NDCs under ANDA 215959
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 Potassiumlosartan | Losartan potassium 25 mg/1 | TabletOral | Granules India Ltd | 62207-741 |
| Losartan Potassiumlosartan | Losartan potassium 100 mg/1 | TabletOral | Granules India Ltd | 62207-743 |
| Losartan Potassiumlosartan | Losartan potassium 50 mg/1 | TabletOral | Preferred Pharmaceuticals Inc. | 68788-4160 |
| Losartan Potassiumlosartan | Losartan potassium 25 mg/1 | TabletOral | Granules Pharmaceuticals Inc. | 70010-741 |
| Losartan Potassiumlosartan | Losartan potassium 50 mg/1 | TabletOral | Granules Pharmaceuticals Inc. | 70010-742 |
| Losartan Potassiumlosartan | Losartan potassium 100 mg/1 | TabletOral | Granules Pharmaceuticals Inc. | 70010-743 |