0052-2139 : Saphris 5 mg Sublingual Tablet
| NDC: | 0052-2139 |
| Labeler: | Organon Pharmaceuticals USA |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Saphris |
| Dosage Form: | Sublingual Tablet |
| Application #: | NDA022117 |
| Rev. Date: |
Appearance:
| Markings: | 5 |
| Shapes: |
Round |
| Colors: |
 White |
| Size (mm): | 12 |
| 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:
- 0052-2139-02: 2 CASE IN 1 CARTON (0052‑2139‑02) > 1 BLISTER PACK IN 1 CASE > 10 TABLET IN 1 BLISTER PACK
- 0052-2139-03: 6 CASE IN 1 CARTON (0052‑2139‑03) > 1 BLISTER PACK IN 1 CASE > 10 TABLET IN 1 BLISTER PACK
- 0052-2139-04: 10 BLISTER PACK IN 1 CARTON (0052‑2139‑04) > 10 TABLET IN 1 BLISTER PACK
Active Ingredients:
- Asenapine Maleate
Dosage Strength:
- 5 mg
Inactive Ingredients:
- Gelatin
- Mannitol
- Sucralose
Pharmaceutical Classes:
- Atypical Antipsychotic [EPC]
Related Products:
Based on records with the same trade name.- 0052-0118 Saphris 5 mg Sublingual Tablet by Organon Pharmaceuticals USA
- 0052-0119 Saphris 10 mg Sublingual Tablet by Organon Pharmaceuticals USA
- 0052-2142 Saphris 10 mg Sublingual Tablet by Organon Pharmaceuticals USA
- 0456-2402 Saphris 2.5 mg Sublingual Tablet by Forest Laboratories, Inc.
- 0456-2405 Saphris 5 mg Sublingual Tablet by Forest Laboratories, Inc.
- 0456-2410 Saphris 10 mg Sublingual Tablet by Forest Laboratories, Inc.
- 16590-936 Saphris 10 mg Sublingual Tablet by Stat Rx USA 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.