0574-0215 : Naratriptan (As Naratriptan Hydrochloride) 2.5 mg Oral Tablet
| NDC: | 0574-0215 |
| Labeler: | Paddock Laboratories, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Naratriptan Hydrochloride |
| Dosage Form: | Oral Tablet, Film Coated |
| Application #: | ANDA091326 |
| Rev. Date: |
Appearance:
| Markings: | PAD;215 |
| Shapes: |
Round |
| Colors: |
 Green |
| Size (mm): | 4 |
| 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:
- 0574-0215-09: 1 BLISTER PACK IN 1 CARTON (0574‑0215‑09) > 9 TABLET, FILM COATED IN 1 BLISTER PACK
Active Ingredients:
- Naratriptan Hydrochloride
Dosage Strength:
- 2.5 mg
Inactive Ingredients:
- Croscarmellose Sodium
- Anhydrous Lactose
- Magnesium Stearate
- Cellulose, Microcrystalline
- Hypromellose
- D&c Yellow No. 10
- Fd&c Blue No. 1
- Aluminum Oxide
- Fd&c Red No. 40
- Titanium Dioxide
- Triacetin
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.- 0574-0214 Naratriptan (As Naratriptan Hydrochloride) 1 mg Oral Tablet by Paddock Laboratories, Inc.
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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.