rizatriptan benzoate

Generic: rizatriptan benzoate

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name rizatriptan benzoate
Generic Name rizatriptan benzoate
Labeler rising pharma holdings, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

rizatriptan benzoate 5 mg/1

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 57237-087
Product ID 57237-087_1bef187c-7644-4b06-b4cb-f73499d65bdf
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202490
Listing Expiration 2026-12-31
Marketing Start 2012-12-31

Pharmacologic Class

Classes
serotonin 1b receptor agonists [moa] serotonin 1d receptor agonists [moa] serotonin-1b and serotonin-1d receptor agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 57237087
Hyphenated Format 57237-087

Supplemental Identifiers

RxCUI
312840 314209
UNII
WR978S7QHH

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name rizatriptan benzoate (source: ndc)
Generic Name rizatriptan benzoate (source: ndc)
Application Number ANDA202490 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 4 BLISTER PACK in 1 CARTON (57237-087-34) / 3 TABLET in 1 BLISTER PACK
  • 3 BLISTER PACK in 1 CARTON (57237-087-63) / 6 TABLET in 1 BLISTER PACK
source: ndc

Packages (2)

57237-087-34 4 BLISTER PACK in 1 CARTON (57237-087-34) / 3 TABLET in 1 BLISTER PACK 57237-087-63 3 BLISTER PACK in 1 CARTON (57237-087-63) / 6 TABLET in 1 BLISTER PACK

Ingredients (1)

rizatriptan benzoate (5 mg/1)

Linked Drug Pages (1)

Rizatriptan Benzoate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1bef187c-7644-4b06-b4cb-f73499d65bdf", "openfda": {"unii": ["WR978S7QHH"], "rxcui": ["312840", "314209"], "spl_set_id": ["222f77ff-d3f7-40f9-989c-e5902f44ef1e"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 BLISTER PACK in 1 CARTON (57237-087-34)  / 3 TABLET in 1 BLISTER PACK", "package_ndc": "57237-087-34", "marketing_start_date": "20121231"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (57237-087-63)  / 6 TABLET in 1 BLISTER PACK", "package_ndc": "57237-087-63", "marketing_start_date": "20121231"}], "brand_name": "Rizatriptan Benzoate", "product_id": "57237-087_1bef187c-7644-4b06-b4cb-f73499d65bdf", "dosage_form": "TABLET", "pharm_class": ["Serotonin 1b Receptor Agonists [MoA]", "Serotonin 1d Receptor Agonists [MoA]", "Serotonin-1b and Serotonin-1d Receptor Agonist [EPC]"], "product_ndc": "57237-087", "generic_name": "Rizatriptan Benzoate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rizatriptan Benzoate", "active_ingredients": [{"name": "RIZATRIPTAN BENZOATE", "strength": "5 mg/1"}], "application_number": "ANDA202490", "marketing_category": "ANDA", "marketing_start_date": "20121231", "listing_expiration_date": "20261231"}