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United States · US · US:71335-2485_7f075beb-f2b7-40e2-a4f4-a220bf1a2ac7

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 · 10

  • ndc11
    7133524850
    28 TABLET in 1 BOTTLE (71335-2485-0)
  • ndc11
    7133524851
    30 TABLET in 1 BOTTLE (71335-2485-1)
  • ndc11
    7133524852
    60 TABLET in 1 BOTTLE (71335-2485-2)
  • ndc11
    7133524853
    10 TABLET in 1 BOTTLE (71335-2485-3)
  • ndc11
    7133524854
    90 TABLET in 1 BOTTLE (71335-2485-4)
  • ndc11
    7133524855
    20 TABLET in 1 BOTTLE (71335-2485-5)
  • ndc11
    7133524856
    120 TABLET in 1 BOTTLE (71335-2485-6)
  • ndc11
    7133524857
    14 TABLET in 1 BOTTLE (71335-2485-7)
  • ndc11
    7133524858
    42 TABLET in 1 BOTTLE (71335-2485-8)
  • ndc11
    7133524859
    40 TABLET in 1 BOTTLE (71335-2485-9)

Annotations

UNII (FDA Substance ID)
57Y76R9ATQ
NAPROXEN
RxCUI 7258
Orange Book
A078250
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "57Y76R9ATQ",
    "rxcui": "7258",
    "inchikey": "CMWTZPSULFXXJA-VIFPVBQESA-N",
    "display_name": "NAPROXEN",
    "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": "71335-2485_7f075beb-f2b7-40e2-a4f4-a220bf1a2ac7",
  "productndc": "71335-2485",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "078250",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "250MG",
        "product_no": "001",
        "approval_date": "Mar 28, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "375MG",
        "product_no": "002",
        "approval_date": "Mar 28, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "500MG",
        "product_no": "003",
        "approval_date": "Mar 28, 2007"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "NAPROXEN",
  "proprietary_name": "Naproxen",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078250",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Naproxen",
  "start_marketing_date": "20070701",
  "active_numerator_strength": "500"
}

Related drugs

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