Search by Drug Name or NDC
NDC 29300-0317-21 Rizatriptan Benzoate 10 mg/1 Details
Rizatriptan Benzoate 10 mg/1
Rizatriptan Benzoate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Unichem Pharmaceuticals (USA), Inc.. The primary component is RIZATRIPTAN BENZOATE.
MedlinePlus Drug Summary
Rizatriptan is used to treat the symptoms of migraine headaches (severe, throbbing headaches that sometimes are accompanied by nausea and sensitivity to sound and light). Rizatriptan is in a class of medications called selective serotonin receptor agonists. It works by narrowing blood vessels in the brain, stopping pain signals from being sent to the brain, and blocking the release of certain natural substances that cause pain, nausea, and other symptoms of migraine. Rizatriptan does not prevent migraine attacks or reduce the number of headaches you have.
Related Packages: 29300-0317-21Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Rizatriptan
Product Information
| NDC | 29300-0317 |
|---|---|
| Product ID | 29300-317_b86514bb-961e-4cf9-9f52-d5f441b7c97f |
| Associated GPIs | 67406060100320 |
| GCN Sequence Number | 040222 |
| GCN Sequence Number Description | rizatriptan benzoate TABLET 10 MG ORAL |
| HIC3 | H3F |
| HIC3 Description | ANTIMIGRAINE PREPARATIONS |
| GCN | 19592 |
| HICL Sequence Number | 018535 |
| HICL Sequence Number Description | RIZATRIPTAN BENZOATE |
| Brand/Generic | Generic |
| Proprietary Name | Rizatriptan Benzoate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Rizatriptan Benzoate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | RIZATRIPTAN BENZOATE |
| Labeler Name | Unichem Pharmaceuticals (USA), Inc. |
| Pharmaceutical Class | Serotonin 1b Receptor Agonists [MoA], Serotonin 1d Receptor Agonists [MoA], Serotonin-1b and Serotonin-1d Receptor Agonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA207836 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 29300-0317-21 (29300031721)
| NDC Package Code | 29300-317-21 |
|---|---|
| Billing NDC | 29300031721 |
| Package | 4 BLISTER PACK in 1 CARTON (29300-317-21) / 3 TABLET in 1 BLISTER PACK (29300-317-31) |
| Marketing Start Date | 2017-07-05 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |