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United States · US · US:71335-3009_884dc6b0-d277-4c9b-8270-acc2abacff6c

Rugby All Day Relief

Orange BookUNIISPLATC G02CC02

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

Identification

ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeG02CC02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 9

  • ndc11
    7133530091
    20 TABLET, FILM COATED in 1 BOTTLE (71335-3009-1)
  • ndc11
    7133530092
    30 TABLET, FILM COATED in 1 BOTTLE (71335-3009-2)
  • ndc11
    7133530093
    40 TABLET, FILM COATED in 1 BOTTLE (71335-3009-3)
  • ndc11
    7133530094
    50 TABLET, FILM COATED in 1 BOTTLE (71335-3009-4)
  • ndc11
    7133530095
    60 TABLET, FILM COATED in 1 BOTTLE (71335-3009-5)
  • ndc11
    7133530096
    14 TABLET, FILM COATED in 1 BOTTLE (71335-3009-6)
  • ndc11
    7133530097
    100 TABLET, FILM COATED in 1 BOTTLE (71335-3009-7)
  • ndc11
    7133530098
    90 TABLET, FILM COATED in 1 BOTTLE (71335-3009-8)
  • ndc11
    7133530099
    24 TABLET, FILM COATED in 1 BOTTLE (71335-3009-9)

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": {
    "50c46cf5-3e64-9e0f-e063-6294a90a2317": {
      "match": "brand_token",
      "title": "RUGBY ANTIFUNGAL (TOLNAFTATE AEROSOL, POWDER) AEROSOL, SPRAY [RUGBY LABORATORIES]",
      "spl_version": "2",
      "published_date": "2026-05-20"
    }
  },
  "productid": "71335-3009_884dc6b0-d277-4c9b-8270-acc2abacff6c",
  "productndc": "71335-3009",
  "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 PRESCRIPTION DRUG",
  "substance_name": "NAPROXEN SODIUM",
  "proprietary_name": "Rugby All Day Relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA074661",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Naproxen Sodium",
  "start_marketing_date": "20150902",
  "active_numerator_strength": "220"
}

Related drugs

Other records sharing ATC code G02CC02.

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