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United States · US · US:71335-0100_ca06cd0b-6979-4948-91c4-8635aec581c9

Loratadine Allergy Relief

Orange BookUNIISPLATC R06AX13

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeR06AX13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 9

  • ndc11
    7133501001
    20 TABLET in 1 BOTTLE (71335-0100-1)
  • ndc11
    7133501002
    30 TABLET in 1 BOTTLE (71335-0100-2)
  • ndc11
    7133501003
    60 TABLET in 1 BOTTLE (71335-0100-3)
  • ndc11
    7133501004
    14 TABLET in 1 BOTTLE (71335-0100-4)
  • ndc11
    7133501005
    10 TABLET in 1 BOTTLE (71335-0100-5)
  • ndc11
    7133501006
    90 TABLET in 1 BOTTLE (71335-0100-6)
  • ndc11
    7133501007
    28 TABLET in 1 BOTTLE (71335-0100-7)
  • ndc11
    7133501008
    15 TABLET in 1 BOTTLE (71335-0100-8)
  • ndc11
    7133501009
    100 TABLET in 1 BOTTLE (71335-0100-9)

Annotations

UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A076134
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": {
    "d778c4d2-184a-4dc8-9351-66d81d0618f2": {
      "match": "brand_token",
      "title": "LORATADINE TABLET [PREFERRED PHARMACEUTICALS INC.]",
      "spl_version": "3",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-0100_ca06cd0b-6979-4948-91c4-8635aec581c9",
  "productndc": "71335-0100",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "076134",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Aug 18, 2003"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LORATADINE",
  "proprietary_name": "Loratadine Allergy Relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA076134",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Loratadine",
  "start_marketing_date": "20171101",
  "active_numerator_strength": "10"
}

Related drugs

Other records sharing ATC code R06AX13.

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