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United States · US · US:69230-329_ee21e0f7-9f32-6c63-e053-2a95a90ac996

Naproxen sodium

Orange BookUNIISPLATC G02CC02

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

Identification

ManufacturerCamber Consumer Care Inc
CountryUS (United States)
ATC codeG02CC02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    6923032901
    1 BOTTLE in 1 CARTON (69230-329-01) / 100 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    6923032902
    1 BOTTLE in 1 CARTON (69230-329-02) / 200 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    6923032905
    500 TABLET, FILM COATED in 1 BOTTLE (69230-329-05)
  • ndc11
    6923032910
    1000 TABLET, FILM COATED in 1 BOTTLE (69230-329-10)
  • ndc11
    6923032924
    1 BOTTLE in 1 CARTON (69230-329-24) / 24 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    6923032950
    1 BOTTLE in 1 CARTON (69230-329-50) / 50 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A211065
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": "69230-329_ee21e0f7-9f32-6c63-e053-2a95a90ac996",
  "productndc": "69230-329",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "211065",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "220MG",
        "product_no": "001",
        "approval_date": "Oct 28, 2022"
      }
    ],
    "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": "ANDA211065",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Naproxen sodium",
  "start_marketing_date": "20221028",
  "active_numerator_strength": "220"
}

Related drugs

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