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United States · US · US:0363-1612_511ca689-d11e-4aeb-b55d-a2d01e20060a

allergy relief

Orange BookUNIISPLATC R06AX13

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

Identification

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

Packs · 8

  • ndc11
    0363161295
    1 BOTTLE in 1 CARTON (0363-1612-95) / 45 TABLET in 1 BOTTLE
  • ndc11
    0363161203
    1 BOTTLE in 1 CARTON (0363-1612-03) / 70 TABLET in 1 BOTTLE
  • ndc11
    0363161247
    1 BOTTLE in 1 CARTON (0363-1612-47) / 150 TABLET in 1 BOTTLE
  • ndc11
    0363161258
    1 BOTTLE in 1 CARTON (0363-1612-58) / 40 TABLET in 1 BOTTLE
  • ndc11
    0363161265
    1 BOTTLE in 1 CARTON (0363-1612-65) / 30 TABLET in 1 BOTTLE
  • ndc11
    0363161275
    1 BOTTLE in 1 CARTON (0363-1612-75) / 90 TABLET in 1 BOTTLE
  • ndc11
    0363161278
    1 BOTTLE in 1 CARTON (0363-1612-78) / 100 TABLET in 1 BOTTLE
  • ndc11
    0363161288
    1 BOTTLE in 1 CARTON (0363-1612-88) / 365 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": "0363-1612_511ca689-d11e-4aeb-b55d-a2d01e20060a",
  "productndc": "0363-1612",
  "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": "20211021",
  "active_numerator_strength": "10"
}

Related drugs

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