67618-120 : Senokot 17.2 mg Oral Tablet
NDC: | 67618-120 |
Labeler: | Purdue Products Lp |
Product Type: | Human OTC Drug |
Drug Name: | Senokot |
Dosage Form: | Oral Tablet |
Application #: | part334 |
Rev. Date: |
Appearance:
Markings: | X |
Shapes: |
Round |
Colors: |
Brown |
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. |
NDC Package Codes:
- 67618-120-06: 36 TABLET, FILM COATED IN 1 BOTTLE (67618‑120‑06)
- 67618-120-12: 1 BLISTER PACK IN 1 CARTON (67618‑120‑12) > 12 TABLET IN 1 BLISTER PACK
- 67618-120-36: 3 BLISTER PACK IN 1 CELLO PACK (67618‑120‑36) > 12 BLISTER PACK IN 1 BLISTER PACK > 12 TABLET IN 1 BLISTER PACK
Active Ingredients:
- Sennosides
Dosage Strength:
- 17.2 mg
Inactive Ingredients:
- Croscarmellose Sodium
- Anhydrous Dibasic Calcium Phosphate
- Hypromellose, Unspecified
- Lactose, Unspecified Form
- Magnesium Stearate
- Microcrystalline Cellulose
- Mineral Oil
- Stearic Acid
- Tartaric Acid
Related Products:
Based on records with the same trade name.- 67618-300 Senokot 8.6 mg Oral Tablet by Purdue Products Lp
- 67618-371 Senokot 8.6 mg Oral Tablet by Avrio Health L.p.
- 69189-0421 Senokot 8.6 mg Oral Tablet by Avera Mckennan Hospital
NDC QR Code
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Senokot S
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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.