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United States · US · US:70000-0171_b063c471-3082-43b3-8fc5-ece0715c6df4

Leader All Day Pain Relief

Orange BookUNIISPLATC G02CC02

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

Identification

ManufacturerCardinal Health 110, LLC. dba Leader
CountryUS (United States)
ATC codeG02CC02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    7000001713
    1 BOTTLE in 1 CARTON (70000-0171-3) / 50 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    7000001715
    1 BOTTLE in 1 CARTON (70000-0171-5) / 24 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    7000001716
    1 BOTTLE in 1 CARTON (70000-0171-6) / 90 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A074661
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "9TN87S3A3C",
    "rxcui": "142442",
    "inchikey": "CDBRNDSHEYLDJV-FVGYRXGTSA-M",
    "display_name": "NAPROXEN SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "12971fb2-2314-4443-bf70-b7eb5859b148": {
      "match": "brand_token",
      "title": "LEADER MUCUS RELIEF D (GUAIFENESIN, PSEUDOEPHEDRINE HYDROCHLORIDE) TABLET, MULTILAYER, EXTENDED RELEASE [CARDINAL HEALTH 110, LLC. DBA LEADER]",
      "spl_version": "3",
      "published_date": "2026-06-01"
    }
  },
  "productid": "70000-0171_b063c471-3082-43b3-8fc5-ece0715c6df4",
  "productndc": "70000-0171",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "074661",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "220MG",
        "product_no": "001",
        "approval_date": "Jan 13, 1997"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "NAPROXEN SODIUM",
  "proprietary_name": "Leader All Day Pain Relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA074661",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Naproxen Sodium",
  "start_marketing_date": "20161129",
  "active_numerator_strength": "220"
}

Related drugs

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