Prescription drug · ANDA
Sertraline Hydrochloride NDC 70771-1914
Sertraline hydrochloride 200 mg/1 · Capsule · Oral · Zydus Lifesciences Limited
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 70771-1914-3 | 7077119140370771191403 | 30 CAPSULE in 1 BOTTLE (70771-1914-3)Marketed from Jan 29, 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)
- Sertraline Hydrochloride
- Generic name (nonproprietary)
- sertraline hydrochloride
- Active ingredients
- Sertraline hydrochloride — 200 mg/1
- Dosage form
- Capsule
- Route
- Oral
- Labeler
- Zydus Lifesciences LimitedNDC labeler code 70771
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 220275
- Marketing start
- Listing expires
- Other FDA classes
- Cytochrome P450 2D6 Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
- Identifiers
- Product ID 70771-1914_e5ff2f30-1085-40b7-a090-a8393a7c422fSPL ID e5ff2f30-1085-40b7-a090-a8393a7c422fSPL set ID 96dedceb-81ad-447c-800e-800cf473d4e4RxCUI 251201, 410584UNII UTI8907Y6X
- 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
N470771191403followed by a unit qualifier and the quantityPackage 70771-1914-03. 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)
Sertraline hydrochloride capsules are indicated for the treatment of the following [see Clinical Studies ( 14 )] : Major depressive disorder (MDD) in adults Obsessive-compulsive disorder (OCD) in adults and pediatric patients 6 years and older Sertraline hydrochloride capsules are a selective serotonin reuptake inhibitor (SSRI) indicated for the treatment of ( 1 ): Major depressive disorder (MDD) in adults Obsessive-compulsive disorder (OCD) in adults and pediatric patients 6 years and older
Excerpt only. Read the full label for complete information.
About NDC 70771-1914
- What is NDC 70771-1914?
- 70771-1914 is the product NDC for Sertraline Hydrochloride, Sertraline hydrochloride 200 mg/1 capsule, listed with the FDA by Zydus Lifesciences Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Sertraline Hydrochloride.
- What is the active ingredient?
- Sertraline hydrochloride.
- Who is the labeler?
- Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Sertraline Hydrochloride?
- 182 other product NDCs are listed under this name. See all Sertraline Hydrochloride NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Sertraline Hydrochloride products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Sertraline Hydrochloride | Sertraline hydrochloride 150 mg/1 | Tablet, Film coatedOral | TRUPHARMA, LLC | 52817-223 | 52817-0223-90 |
| Sertraline Hydrochloride | Sertraline hydrochloride 200 mg/1 | Tablet, Film coatedOral | TRUPHARMA, LLC | 52817-224 | 52817-0224-90 |
| Sertraline hydrochloride | Sertraline hydrochloride 100 mg/1 | Tablet, Film coatedOral | REMEDYREPACK INC. | 70518-4707 | 70518-4707-0070518-4707-02 |
| Sertraline Hydrochloride | Sertraline hydrochloride 50 mg/1 | Tablet, Film coatedOral | Preferred Pharmaceuticals Inc. | 68788-4151 | 68788-4151-0168788-4151-0368788-4151-06+1 more |
| Sertraline Hydrochloride | Sertraline hydrochloride 25 mg/1 | TabletOral | Coupler LLC | 67046-1181 | 67046-1181-03 |
| Sertraline Hydrochloride | Sertraline hydrochloride 100 mg/1 | Tablet, Film coatedOral | Unit Dose Solutions, Inc. | 87441-076 | 87441-0076-01 |
| Sertraline Hydrochloride | Sertraline hydrochloride 50 mg/1 | Tablet, Film coatedOral | Unit Dose Solutions, Inc. | 87441-077 | 87441-0077-01 |
| Sertraline Hydrochloride | Sertraline hydrochloride 25 mg/1 | Tablet, Film coatedOral | Unit Dose Solutions, Inc. | 87441-075 | 87441-0075-01 |
| Sertraline hydrochloride | Sertraline hydrochloride 100 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-1682 | 67046-1682-03 |
| Sertraline Hydrochloride | Sertraline hydrochloride 50 mg/1 | Tablet, Film coatedOral | Coupler LLC | 67046-0555 | 67046-0555-03 |
Other NDCs under ANDA 220275
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 |
|---|---|---|---|---|
| Sertraline Hydrochloride | Sertraline hydrochloride 150 mg/1 | CapsuleOral | Zydus Pharmaceuticals (USA) Inc. | 70710-1948 |
| Sertraline Hydrochloride | Sertraline hydrochloride 200 mg/1 | CapsuleOral | Zydus Pharmaceuticals (USA) Inc. | 70710-1949 |
| Sertraline Hydrochloride | Sertraline hydrochloride 150 mg/1 | CapsuleOral | Zydus Lifesciences Limited | 70771-1913 |