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United States · US · US:50844-714_bc397444-6e0e-4b4e-8f03-d6372588d8ab

Naproxen Back and Muscle Pain

Orange BookUNIISPLATC G02CC02

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

Identification

ManufacturerL.N.K. International, Inc.
CountryUS (United States)
ATC codeG02CC02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    5084471414
    500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-14)
  • ndc11
    5084471416
    1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-16)
  • ndc11
    5084471419
    1 BOTTLE, PLASTIC in 1 CARTON (50844-714-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
  • ndc11
    5084471456
    25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-56)
  • ndc11
    5084471498
    8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-98)
  • ndc11
    5084471499
    8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-99)

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": "50844-714_bc397444-6e0e-4b4e-8f03-d6372588d8ab",
  "productndc": "50844-714",
  "dosage_form": "TABLET, FILM COATED",
  "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 Back and Muscle Pain",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA204872",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Naproxen Sodium",
  "start_marketing_date": "20190201",
  "active_numerator_strength": "220"
}

Related drugs

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