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United States · US · US:33342-087_fe80232a-c329-47ed-8edd-7786e06f3c08

Rizatriptan

Orange BookUNIISPLATC N02CC04

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerMacleods Pharmaceuticals Limited
CountryUS (United States)
ATC codeN02CC04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 7

  • ndc11
    3334208707
    30 TABLET, FILM COATED in 1 CONTAINER (33342-087-07)
  • ndc11
    3334208712
    10 BLISTER PACK in 1 CARTON (33342-087-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    3334208741
    3 BLISTER PACK in 1 CARTON (33342-087-41) / 6 TABLET, FILM COATED in 1 BLISTER PACK (33342-087-02)
  • ndc11
    3334208745
    2 BLISTER PACK in 1 CARTON (33342-087-45) / 6 TABLET, FILM COATED in 1 BLISTER PACK (33342-087-02)
  • ndc11
    3334208746
    200 TABLET, FILM COATED in 1 CONTAINER (33342-087-46)
  • ndc11
    3334208750
    4 BLISTER PACK in 1 CARTON (33342-087-50) / 3 TABLET, FILM COATED in 1 BLISTER PACK (33342-087-52)
  • ndc11
    3334208772
    6 BLISTER PACK in 1 CARTON (33342-087-72) / 3 TABLET, FILM COATED in 1 BLISTER PACK (33342-087-52)

Annotations

UNII (FDA Substance ID)
WR978S7QHH
RIZATRIPTAN BENZOATE
RxCUI 237082
Orange Book
A203147
ABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "WR978S7QHH",
    "rxcui": "237082",
    "inchikey": "JPRXYLQNJJVCMZ-UHFFFAOYSA-N",
    "display_name": "RIZATRIPTAN BENZOATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "f754388d-77f1-0d8d-e053-6394a90a7b7e": {
      "match": "brand_token",
      "title": "RIZATRIPTAN BENZOATE TABLET, FILM COATED [DIRECT_RX]",
      "spl_version": "4",
      "published_date": "2026-03-18"
    }
  },
  "productid": "33342-087_fe80232a-c329-47ed-8edd-7786e06f3c08",
  "productndc": "33342-087",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "203147",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 5MG BASE",
        "product_no": "001",
        "approval_date": "Feb 11, 2014"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE",
        "product_no": "002",
        "approval_date": "Feb 11, 2014"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "RIZATRIPTAN BENZOATE",
  "proprietary_name": "Rizatriptan",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA203147",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Rizatriptan",
  "start_marketing_date": "20140311",
  "active_numerator_strength": "5"
}

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