0591-5716 : Amoxapine 150 mg Oral Tablet
| NDC: | 0591-5716 |
| Labeler: | Watson Laboratories, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Amoxapine |
| Dosage Form: | Oral Tablet |
| Application #: | ANDA072691 |
| Rev. Date: |
Appearance:
| Markings: | DAN;150;5716 |
| Shapes: |
Round |
| Colors: |
 Orange |
| Size (mm): | 10 |
| Segments: * | 2 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces. | |
NDC Package Codes:
- 0591-5716-30: 30 TABLET IN 1 BOTTLE, PLASTIC (0591‑5716‑30)
Active Ingredients:
- Amoxapine
Dosage Strength:
- 150 mg
Inactive Ingredients:
- Dibasic Calcium Phosphate Dihydrate
- Magnesium Stearate
- Starch, Corn
- Stearic Acid
- Fd&c Yellow No. 6
Pharmaceutical Classes:
- Tricyclic Antidepressant [EPC]
Related Products:
Based on records with the same trade name.- 0591-5713 Amoxapine 25 mg Oral Tablet by Watson Laboratories, Inc.
- 0591-5714 Amoxapine 50 mg Oral Tablet by Watson Laboratories, Inc.
- 0591-5715 Amoxapine 100 mg Oral Tablet by Watson Laboratories, Inc.
- 54868-2438 Amoxapine 50 mg Oral Tablet by Physicians Total Care, Inc.
- 62135-700 Amoxapine 25 mg Oral Tablet by Chartwell Rx, LLC
- 62135-701 Amoxapine 50 mg Oral Tablet by Chartwell Rx, LLC
- 62135-702 Amoxapine 100 mg Oral Tablet by Chartwell Rx, LLC
- 62135-703 Amoxapine 150 mg Oral Tablet by Chartwell Rx, LLC
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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.