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United States · US · US:71335-2584_ad5331f1-30bc-489e-95ba-e791512ba4aa

Good Sense Naproxen Sodium

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
    7133525841
    20 TABLET, FILM COATED in 1 BOTTLE (71335-2584-1)
  • ndc11
    7133525842
    30 TABLET, FILM COATED in 1 BOTTLE (71335-2584-2)
  • ndc11
    7133525843
    40 TABLET, FILM COATED in 1 BOTTLE (71335-2584-3)
  • ndc11
    7133525844
    50 TABLET, FILM COATED in 1 BOTTLE (71335-2584-4)
  • ndc11
    7133525845
    60 TABLET, FILM COATED in 1 BOTTLE (71335-2584-5)
  • ndc11
    7133525846
    14 TABLET, FILM COATED in 1 BOTTLE (71335-2584-6)
  • ndc11
    7133525847
    100 TABLET, FILM COATED in 1 BOTTLE (71335-2584-7)
  • ndc11
    7133525848
    90 TABLET, FILM COATED in 1 BOTTLE (71335-2584-8)
  • ndc11
    7133525849
    24 TABLET, FILM COATED in 1 BOTTLE (71335-2584-9)

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": {
    "d503b10f-85cd-4bb8-9dec-82d651d525fa": {
      "match": "brand_token",
      "title": "GOOD NEIGHBOR PHARMACY EARWAX REMOVAL (CARBAMIDE PEROXIDE) KIT [AMERISOURCE BERGEN]",
      "spl_version": "3",
      "published_date": "2026-06-01"
    }
  },
  "productid": "71335-2584_ad5331f1-30bc-489e-95ba-e791512ba4aa",
  "productndc": "71335-2584",
  "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": "Good Sense Naproxen Sodium",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA074661",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Naproxen Sodium",
  "start_marketing_date": "20140331",
  "active_numerator_strength": "220"
}

Related drugs

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