0615-8083 : Senexon-s Oral Tablet, Coated
| NDC: | 0615-8083 |
| Labeler: | Ncs Healthcare of Ky, Inc Dba Vangard Labs |
| Product Type: | Human OTC Drug |
| Drug Name: | Senexon-s |
| Dosage Form: | Oral Tablet, Coated |
| Application #: | part334 |
| Rev. Date: |
Appearance:
| Markings: | TCL081 |
| Shapes: |
Round |
| Colors: |
 Orange |
| Size (mm): | 9 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 0615-8083-39: 30 TABLET, COATED IN 1 BLISTER PACK (0615‑8083‑39)
Active Ingredients:
- Docusate Sodium
- Sennosides a and B
Dosage Strength:
- 50 mg
- 8.6 mg
Inactive Ingredients:
- Carnauba Wax
- Silicon Dioxide
- Croscarmellose Sodium
- D&c Yellow No. 10
- Dibasic Calcium Phosphate Dihydrate
- Fd&c Yellow No. 6
- Hypromelloses
- Magnesium Stearate
- Cellulose, Microcrystalline
- Polyethylene Glycols
- Sodium Benzoate
- Stearic Acid
- Titanium Dioxide
Related Products:
Based on records with the same trade name.- 0615-7773 Senexon-s (Docusate Sodium 50 mg / Sennosides, Usp 8.6 mg) Oral Tablet by Ncs Healthcare of Ky, Inc Dba Vangard Labs
- 0615-8331 Senexon-s Oral Tablet, Film Coated by Ncs Healthcare of Ky, Inc Dba Vangard Labs
- 0536-1247 Senexon-s Oral Tablet, Film Coated by Rugby Laboratories
- 0536-4086 Senexon-s (Docusate Sodium 50 mg / Sennosides, Usp 8.6 mg) Oral Tablet by Rugby Laboratories, Inc.
- 33261-749 Senexon-s Oral Tablet, Coated by Aidarex Pharmaceuticals LLC
- 52959-675 Senexon-s (Docusate Sodium 50 mg / Sennosides, Usp 8.6 mg) Oral Tablet by H.j. Harkins Company, Inc.
- 55154-6816 Senexon-s Oral Tablet, Coated by Cardinal Health
- 68788-9407 Senexon-s Oral Tablet, Coated by Preferred Pharmaceuticals, Inc.
- 76237-315 Senexon-s (Docusate Sodium 50 mg / Sennosides, Usp 8.6 mg) Oral Tablet by Mckesson Contract Packaging
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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.
