70518-3322 : Fluoxetine 20 mg Oral Capsule
NDC: | 70518-3322 |
Labeler: | Remedyrepack Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Fluoxetine |
Dosage Form: | Oral Capsule |
Application #: | ANDA204597 |
Rev. Date: |
NDC Package Codes:
- 70518-3322-0: 30 CAPSULE IN 1 BLISTER PACK (70518‑3322‑0)
Active Ingredients:
- Fluoxetine Hydrochloride
Dosage Strength:
- 20 mg
Pharmaceutical Classes:
- Serotonin Reuptake Inhibitor [EPC]
- Serotonin Uptake Inhibitors [MoA]
Related Products:
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- 70518-1359 Fluoxetine 20 mg Oral Capsule by Remedyrepack Inc.
- 70518-1432 Fluoxetine 20 mg Oral Capsule by Remedyrepack Inc.
- 70518-1619 Fluoxetine 20 mg Oral Capsule by Remedyrepack Inc.
- 70518-1757 Fluoxetine 10 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 70518-1775 Fluoxetine 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 70518-1987 Fluoxetine 40 mg Oral Capsule by Remedyrepack Inc.
- 70518-2134 Fluoxetine 40 mg Oral Capsule by Remedyrepack Inc.
- 70518-2162 Fluoxetine 20 mg Oral Tablet, Film Coated by Remedyrepack Inc.
- 70518-2754 Fluoxetine 10 mg Oral Capsule by Remedyrepack Inc.
- 70518-3483 Fluoxetine 10 mg Oral Capsule by Remedyrepack Inc.
- 70518-3554 Fluoxetine 40 mg Oral Capsule by Remedyrepack Inc.
- 70518-3752 Fluoxetine 10 mg Oral Capsule by Remedyrepack Inc.
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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.