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United States · US · US:37808-847_5857482f-bc9f-472a-b86b-ec2e2b83f6dc

allergy relief

Orange BookUNIISPLATC R06AX26

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

Identification

ManufacturerH E B
CountryUS (United States)
ATC codeR06AX26
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    3780884722
    15 BLISTER PACK in 1 CARTON (37808-847-22) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    3780884739
    1 BOTTLE in 1 CARTON (37808-847-39) / 30 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    3780884749
    1 BOTTLE in 1 CARTON (37808-847-49) / 40 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    3780884795
    1 BOTTLE in 1 CARTON (37808-847-95) / 45 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
2S068B75ZU
FEXOFENADINE HYDROCHLORIDE
RxCUI 236474
Orange Book
A212971
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "2S068B75ZU",
    "rxcui": "236474",
    "inchikey": "RRJFVPUCXDGFJB-UHFFFAOYSA-N",
    "display_name": "FEXOFENADINE HYDROCHLORIDE",
    "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": "37808-847_5857482f-bc9f-472a-b86b-ec2e2b83f6dc",
  "productndc": "37808-847",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "212971",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "60MG",
        "product_no": "001",
        "approval_date": "Feb 24, 2020"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "180MG",
        "product_no": "002",
        "approval_date": "Feb 24, 2020"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "FEXOFENADINE HYDROCHLORIDE",
  "proprietary_name": "allergy relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA212971",
  "marketing_category": "ANDA",
  "nonproprietary_name": "fexofenadine hydrochloride",
  "start_marketing_date": "20211222",
  "active_numerator_strength": "180"
}

Related drugs

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