Prescription drug · ANDA
Escitalopram NDC 70518-2317
Escitalopram oxalate 20 mg/1 · Tablet, Film coated · Oral · REMEDYREPACK INC.
NDC codes
FDA NDC DirectoryProduct NDC (as listed)70518-2317Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-2317Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70518-2317-1 | 7051823170170518231701 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2317-1)Marketed from Nov 15, 2019 | |
| 70518-2317-2 | 7051823170270518231702 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2317-2)Marketed from Aug 11, 2020 | |
| 70518-2317-4 | 7051823170470518231704 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2317-4)Marketed from Mar 20, 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)
- Escitalopram
- Generic name (nonproprietary)
- escitalopram
- Active ingredients
- Escitalopram oxalate — 20 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 078032
- Marketing start
- Listing expires
- Other FDA classes
- Serotonin Uptake Inhibitors (Mechanism)
- Identifiers
- Product ID 70518-2317_5cde2828-3a86-bf40-e063-6294a90a3003SPL ID 5cde2828-3a86-bf40-e063-6294a90a3003
- Pharmacologic class
- Serotonin Reuptake Inhibitor
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
N470518231701followed by a unit qualifier and the quantityPackage 70518-2317-01. 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
The FDA listing for this product does not reference a label (SPL) set.
About NDC 70518-2317
- What is NDC 70518-2317?
- 70518-2317 is the product NDC for Escitalopram, Escitalopram oxalate 20 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?
- Escitalopram.
- What is the active ingredient?
- Escitalopram oxalate.
- 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 Escitalopram?
- 108 other product NDCs are listed under this name. See all Escitalopram NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Escitalopram products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-4171 | 68788-4171-0168788-4171-0368788-4171-06+2 more |
| Escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-0355 | 67046-0355-03 |
| Escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4567 | 70518-4567-00 |
| escitalopram | Escitalopram oxalate 15 mg/1 | CapsuleOral | Almatica Pharma LLC | 52427-795 | 52427-0795-30 |
| Escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | American Health Packaging | 60687-865 | 60687-0865-01 |
| escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4300 | 70518-4300-0070518-4300-01 |
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1465 | 67046-1465-03 |
| escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1472 | 67046-1472-03 |
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4239 | 70518-4239-0070518-4239-0170518-4239-02+1 more |
| escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-8723 | 68788-8723-0168788-8723-0368788-8723-06+2 more |
Other NDCs under ANDA 078032
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 |
|---|---|---|---|---|
| Escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | QPharma, Inc. | 42708-155 |
| Escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | QPharma, Inc. | 42708-163 |
| Escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | SOLCO HEALTHCARE US, LLC | 43547-280 |
| Escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | SOLCO HEALTHCARE US, LLC | 43547-281 |
| Escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | SOLCO HEALTHCARE US, LLC | 43547-282 |
| Escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-5312 |
| Escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-6190 |
| Escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-6191 |
| Escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-6534 |
| Escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-6897 |
| Escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-116 |
| Escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-277 |
| Escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | Northwind Health Company, LLC | 51655-284 |
| Escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | American Health Packaging | 60687-865 |
| Escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-0355 |
| Escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | RedPharm Drug, Inc. | 67296-1421 |
| Escitalopram | Escitalopram oxalate 5 mg/1 | Tablet, Film coatedOral | BluePoint Laboratories | 68001-591 |
| Escitalopram | Escitalopram oxalate 10 mg/1 | Tablet, Film coatedOral | BluePoint Laboratories | 68001-592 |
| Escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | BluePoint Laboratories | 68001-593 |
| Escitalopram | Escitalopram oxalate 20 mg/1 | Tablet, Film coatedOral | NuCare Pharmaceuticals,Inc. | 68071-5248 |
Showing 20 of 32.