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United States · US · US:59779-612_4fd50f17-7237-4659-bad6-a9e6189fa37c

allergy relief

Orange BookUNIISPLATC R06AX13

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

Identification

ManufacturerCVS Pharmacy
CountryUS (United States)
ATC codeR06AX13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 8

  • ndc11
    5977961203
    1 BOTTLE in 1 CARTON (59779-612-03) / 70 TABLET in 1 BOTTLE
  • ndc11
    5977961246
    10 BLISTER PACK in 1 CARTON (59779-612-46) / 1 TABLET in 1 BLISTER PACK
  • ndc11
    5977961258
    1 BOTTLE in 1 CARTON (59779-612-58) / 40 TABLET in 1 BOTTLE
  • ndc11
    5977961265
    1 BOTTLE in 1 CARTON (59779-612-65) / 30 TABLET in 1 BOTTLE
  • ndc11
    5977961270
    2 BOTTLE in 1 CARTON (59779-612-70) / 120 TABLET in 1 BOTTLE (59779-612-76)
  • ndc11
    5977961278
    1 BOTTLE in 1 CARTON (59779-612-78) / 100 TABLET in 1 BOTTLE
  • ndc11
    5977961288
    365 TABLET in 1 BOTTLE (59779-612-88)
  • ndc11
    5977961295
    1 BOTTLE in 1 CARTON (59779-612-95) / 45 TABLET in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A076301
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "7AJO3BO7QN",
    "rxcui": "28889",
    "inchikey": "JCCNYMKQOSZNPW-UHFFFAOYSA-N",
    "display_name": "LORATADINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "934c7b91-3cba-47f0-8efa-77216f3f15c4": {
      "match": "brand_token",
      "title": "ALLERGY RELIEF CHILDRENS (DIPHENHYDRAMINE HCL) TABLET, CHEWABLE [AMERISOURCE BERGEN]",
      "spl_version": "14",
      "published_date": "2026-06-01"
    }
  },
  "productid": "59779-612_4fd50f17-7237-4659-bad6-a9e6189fa37c",
  "productndc": "59779-612",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "076301",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Jun 25, 2004"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LORATADINE",
  "proprietary_name": "allergy relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA076301",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Loratadine",
  "start_marketing_date": "20050104",
  "active_numerator_strength": "10"
}

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