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United States · US · US:58602-737_277b3d51-eb63-4d99-91e0-aa44d0cc8053

Naproxen Sodium HEADACHE PAIN

Orange BookUNIISPLATC G02CC02

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

Identification

ManufacturerAurohealth LLC
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 11

  • ndc11
    5860273707
    1 BOTTLE in 1 CARTON (58602-737-07) / 24 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    5860273712
    1 BOTTLE in 1 CARTON (58602-737-12) / 40 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    5860273719
    1 BOTTLE in 1 CARTON (58602-737-19) / 90 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    5860273721
    1 BOTTLE in 1 CARTON (58602-737-21) / 100 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    5860273725
    1 BOTTLE in 1 CARTON (58602-737-25) / 130 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    5860273729
    1 BOTTLE in 1 CARTON (58602-737-29) / 150 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    5860273734
    1 BOTTLE in 1 CARTON (58602-737-34) / 200 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    5860273738
    1 BOTTLE in 1 CARTON (58602-737-38) / 300 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    5860273740
    1 BOTTLE in 1 CARTON (58602-737-40) / 500 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    5860273744
    400 TABLET, FILM COATED in 1 BOTTLE (58602-737-44)
  • ndc11
    5860273778
    1 BOTTLE in 1 CARTON (58602-737-78) / 50 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A205497
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": "58602-737_277b3d51-eb63-4d99-91e0-aa44d0cc8053",
  "productndc": "58602-737",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "205497",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "220MG",
        "product_no": "001",
        "approval_date": "Mar 18, 2016"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "NAPROXEN SODIUM",
  "proprietary_name": "Naproxen Sodium HEADACHE PAIN",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA205497",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Naproxen Sodium",
  "start_marketing_date": "20210714",
  "active_numerator_strength": "220"
}

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