Naproxen Sodium

Orange BookUNIISPLATC G02CC02

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeG02CC02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 8

ndc11
7133510611
20 TABLET, FILM COATED in 1 BOTTLE (71335-1061-1)
ndc11
7133510612
30 TABLET, FILM COATED in 1 BOTTLE (71335-1061-2)
ndc11
7133510613
40 TABLET, FILM COATED in 1 BOTTLE (71335-1061-3)
ndc11
7133510614
50 TABLET, FILM COATED in 1 BOTTLE (71335-1061-4)
ndc11
7133510615
60 TABLET, FILM COATED in 1 BOTTLE (71335-1061-5)
ndc11
7133510616
14 TABLET, FILM COATED in 1 BOTTLE (71335-1061-6)
ndc11
7133510617
100 TABLET, FILM COATED in 1 BOTTLE (71335-1061-7)
ndc11
7133510618
90 TABLET, FILM COATED in 1 BOTTLE (71335-1061-8)

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": {
    "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": "71335-1061_2d9a3970-0a3a-481f-928d-953ab83d4b9b",
  "productndc": "71335-1061",
  "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": "Naproxen Sodium",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA074661",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Naproxen Sodium",
  "start_marketing_date": "20140411",
  "active_numerator_strength": "220"
}

Related drugs

Other records sharing ATC code G02CC02.

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