Prescription drug · ANDA
Sertraline Hydrochloride NDC 16714-601
Sertraline hydrochloride 20 mg/mL · Solution · Oral · NorthStar Rx LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 16714-601-02 | 1671406010216714060102 | 1 BOTTLE, PLASTIC in 1 CARTON (16714-601-02) / 60 mL in 1 BOTTLE, PLASTICMarketed from Oct 31, 2008 |
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)
- Sertraline Hydrochloride
- Generic name (nonproprietary)
- sertraline hydrochloride
- Active ingredients
- Sertraline hydrochloride — 20 mg/mL
- Dosage form
- Solution
- Route
- Oral
- Labeler
- NorthStar Rx LLCNDC labeler code 16714
- Product type
- Prescription drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 078861
- Marketing start
- Listing expires
- Other FDA classes
- Cytochrome P450 2D6 Inhibitors (Mechanism)Serotonin Uptake Inhibitors (Mechanism)
- Identifiers
- Product ID 16714-601_333a4c5b-223c-4bba-aea7-49c56ab5adc8SPL ID 333a4c5b-223c-4bba-aea7-49c56ab5adc8SPL set ID 7f144b68-ae90-483c-b030-f6824662a734RxCUI 861064UNII 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
N416714060102followed by a unit qualifier and the quantityPackage 16714-0601-02. 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 oral solution is indicated for the treatment of the following [See Clinical Studies (14) ] : Major depressive disorder (MDD) Obsessive-compulsive disorder (OCD) Panic disorder (PD) Posttraumatic stress disorder (PTSD) Social anxiety disorder (SAD) Premenstrual dysphoric disorder (PMDD) Sertraline hydrochloride oral solution is a selective serotonin reuptake inhibitor (SSRI) indicated for the treatment of ( 1 ): Major depressive disorder (MDD) Obsessive-compulsive disorder (OCD) Panic disorder (PD) Posttraumatic stress disorder (PTSD) Social anxiety disorder (SAD) Premenstrual dysphoric disorder (PMDD)
Excerpt only. Read the full label for complete information.
About NDC 16714-601
- What is NDC 16714-601?
- 16714-601 is the product NDC for Sertraline Hydrochloride, Sertraline hydrochloride 20 mg/mL solution, listed with the FDA by NorthStar Rx LLC. 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?
- NorthStar Rx LLC, NDC labeler code 16714. 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 078861
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 20 mg/mL | Solution, ConcentrateOral | Rising Pharma Holdings, Inc. | 64980-409 |
| Sertraline Hydrochloride | Sertraline hydrochloride 20 mg/mL | Solution, ConcentrateOral | Aurobindo Pharma Limited | 65862-224 |