Prescription drug · ANDA
Losartan Potassium NDC 70518-0718
Losartan potassium 100 mg/1 · Tablet, Film coated · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-0718-0 | 7051807180070518071800 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0718-0)Marketed from Aug 30, 2017 | |
| 70518-0718-1 | 7051807180170518071801 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0718-1)Marketed from Jul 20, 2018 | |
| 70518-0718-3 | 7051807180370518071803 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0718-3)Marketed from Mar 20, 2025 |
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 — 100 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- REMEDYREPACK INC.NDC labeler code 70518
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 090083
- Marketing start
- Listing expires
- Other FDA classes
- Angiotensin 2 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 70518-0718_5578ed8d-82e9-104d-e063-6294a90a2164SPL ID 5578ed8d-82e9-104d-e063-6294a90a2164SPL set ID 25c93638-7016-47d2-a57c-e4a5245ca41bRxCUI 979480UNII 3ST302B24A
- 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
N470518071800followed by a unit qualifier and the quantityPackage 70518-0718-00. 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
Current FDA label (SPL), effective . This label includes a boxed warning.
Indications (excerpt from the label)
Losartan potassium tablets are an angiotensin II receptor blocker (ARB) indicated for: Treatment of hypertension, to lower blood pressure in adults and children greater than 6 years old. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Reduction of the risk of stroke in patients with hypertension and left ventricular hypertrophy. There is evidence that this benefit does not apply to Black patients. ( 1.2 ) Treatment of diabetic nephropathy with an elevated serum creatinine and proteinuria in patients with type 2 diabetes and a history of hypertension. ( 1.3 ) 1.1 Hypertension Losartan potassium tablets…
Excerpt only. Read the full label for complete information.
About NDC 70518-0718
- What is NDC 70518-0718?
- 70518-0718 is the product NDC for Losartan Potassium, Losartan potassium 100 mg/1 tablet, film coated, listed with the FDA by REMEDYREPACK INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Losartan Potassium.
- What is the active ingredient?
- Losartan potassium.
- Who is the labeler?
- REMEDYREPACK INC., NDC labeler code 70518. 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 090083
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 25 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-2622 |
| Losartan Potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals,Inc. | 68071-4943 |
| Losartan Potassium | Losartan potassium 100 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-791 |
| Losartan Potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-795 |
| Losartan Potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1174 |
| Losartan Potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-6714 |
| Losartan Potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-0245 |
| Losartan Potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1221 |
| Losartan Potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-918 |
| Losartan Potassium | Losartan potassium 100 mg/1 | Tablet, Film coatedOral | Bryant Ranch Prepack | 71335-1235 |
| Losartan Potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 43063-955 |
| Losartan Potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals,Inc. | 68071-5040 |
| Losartan Potassium | Losartan potassium 100 mg/1 | Tablet, Film coatedOral | PD-Rx Pharmaceuticals, Inc. | 43063-954 |
| Losartan Potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals,Inc. | 68071-5041 |
| Losartan Potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 65862-201 |
| Losartan Potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 65862-202 |
| Losartan Potassium | Losartan potassium 100 mg/1 | Tablet, Film coatedOral | Aurobindo Pharma Limited | 65862-203 |
| Losartan Potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | Proficient Rx LP | 71205-281 |
| Losartan Potassium | Losartan potassium 50 mg/1 | Tablet, Film coatedOral | Unit Dose Solutions, Inc. | 87441-053 |
| Losartan Potassium | Losartan potassium 25 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-2132 |
Showing 20 of 24.