58151-601 : Zoloft 20 mg/ml Oral Solution, Concentrate
NDC: | 58151-601 |
Labeler: | Viatris Specialty LLC |
Product Type: | Human Prescription Drug |
Drug Name: | Zoloft |
Dosage Form: | Oral Solution, Concentrate |
Application #: | NDA020990 |
Rev. Date: |
Active Ingredients:
- Sertraline Hydrochloride
Dosage Strength:
- 20 mg/mL
Pharmaceutical Classes:
- Cytochrome P450 2D6 Inhibitors [MoA]
- Serotonin Reuptake Inhibitor [EPC]
- Serotonin Uptake Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 58151-574 Zoloft 25 mg Oral Tablet, Film Coated by Viatris Specialty LLC
- 58151-575 Zoloft 50 mg Oral Tablet, Film Coated by Viatris Specialty LLC
- 58151-576 Zoloft 100 mg Oral Tablet, Film Coated by Viatris Specialty LLC
- 0049-0050 Zoloft 20 mg/ml Oral Solution, Concentrate by Roerig
- 0049-4900 Zoloft 50 mg Oral Tablet by Roerig
- 0049-4910 Zoloft (As Sertraline Hydrochloride) 100 mg Oral Tablet by Roerig
- 0049-4940 Zoloft 20 mg/ml Oral Solution, Concentrate by Roerig
- 0049-4950 Zoloft 20 mg/ml Oral Solution, Concentrate by Roerig
- 0049-4960 Zoloft 25 mg Oral Tablet by Roerig
- 16590-250 Zoloft 50 mg Oral Tablet by Stat Rx USA LLC
- 16590-251 Zoloft (As Sertraline Hydrochloride) 100 mg Oral Tablet by Stat Rx USA LLC
- 49999-292 Zoloft 50 mg Oral Tablet by Lake Erie Medical & Surgical Supply Dba Quality Care Products LLC
- 49999-375 Zoloft (As Sertraline Hydrochloride) 100 mg Oral Tablet by Lake Erie Medical & Surgical Supply Dba Quality Care Products LLC
- 52125-040 Zoloft (As Sertraline Hydrochloride) 100 mg Oral Tablet by Remedyrepack Inc.
- 55154-2709 Zoloft 50 mg Oral Tablet by Cardinal Health
- 55289-409 Zoloft 50 mg Oral Tablet by Pd-rx Pharmaceuticals, Inc.
- 67544-080 Zoloft (As Sertraline Hydrochloride) 100 mg Oral Tablet by Aphena Pharma Solutions - Tennessee, LLC
- 67544-298 Zoloft 50 mg Oral Tablet by Aphena Pharma Solutions - Tennessee, LLC
- 70518-1913 Zoloft 50 mg Oral Tablet, Film Coated by Remedyrepack Inc.
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.