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United States · US · US:71335-1282_1245c4fb-1cb1-42f8-962d-f059c222ed3f

Naproxen

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
    7133512821
    20 TABLET in 1 BOTTLE (71335-1282-1)
  • ndc11
    7133512822
    30 TABLET in 1 BOTTLE (71335-1282-2)
  • ndc11
    7133512823
    40 TABLET in 1 BOTTLE (71335-1282-3)
  • ndc11
    7133512824
    50 TABLET in 1 BOTTLE (71335-1282-4)
  • ndc11
    7133512825
    60 TABLET in 1 BOTTLE (71335-1282-5)
  • ndc11
    7133512826
    14 TABLET in 1 BOTTLE (71335-1282-6)
  • ndc11
    7133512827
    100 TABLET in 1 BOTTLE (71335-1282-7)
  • ndc11
    7133512828
    90 TABLET in 1 BOTTLE (71335-1282-8)
  • ndc11
    7133512829
    24 TABLET in 1 BOTTLE (71335-1282-9)

Annotations

UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A204872
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": {
    "c5146d73-2f34-4dfe-ac29-97071279dc4d": {
      "match": "brand_token",
      "title": "NAPROXEN SODIUM TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]",
      "spl_version": "10",
      "published_date": "2026-05-28"
    }
  },
  "productid": "71335-1282_1245c4fb-1cb1-42f8-962d-f059c222ed3f",
  "productndc": "71335-1282",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "204872",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "220MG",
        "product_no": "001",
        "approval_date": "Jan 23, 2017"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "NAPROXEN SODIUM",
  "proprietary_name": "Naproxen",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA204872",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Naproxen Sodium",
  "start_marketing_date": "20190101",
  "active_numerator_strength": "220"
}

Related drugs

Other records sharing ATC code G02CC02.

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