59762-2322 : Eletriptan 40 mg Oral Tablet, Film Coated
| NDC: | 59762-2322 |
| Labeler: | Greenstone LLC |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Eletriptan |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | NDA021016 |
| Rev. Date: |
Appearance:
| Markings: | REP40;Pfizer |
| Shapes: |
Round |
| Colors: |
 Orange |
| Size (mm): | 8 |
| 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:
- 59762-2322-1: 6 BLISTER PACK IN 1 CARTON (59762‑2322‑1) > 1 TABLET, FILM COATED IN 1 BLISTER PACK
Active Ingredients:
- Eletriptan Hydrobromide
Dosage Strength:
- 40 mg
Inactive Ingredients:
- Microcrystalline Cellulose
- Lactose, Unspecified Form
- Croscarmellose Sodium
- Magnesium Stearate
- Titanium Dioxide
- Hypromellose, Unspecified
- Triacetin
- Fd&c Yellow No. 6
- Aluminum Oxide
Pharmaceutical Classes:
- Serotonin 1b Receptor Agonists [MoA]
- Serotonin 1d Receptor Agonists [MoA]
- Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]
Related Products:
Based on records with the same trade name.- 59762-2321 Eletriptan 20 mg Oral Tablet, Film Coated by Greenstone 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.