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United States · US · US:0280-6080_4526c253-b571-1d84-e063-6394a90ae3f9

Aleve

Orange BookUNIISPLATC G02CC02

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

Identification

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

Packs · 7

  • ndc11
    0280608001
    1 BOTTLE in 1 CARTON (0280-6080-01) / 120 CAPSULE, LIQUID FILLED in 1 BOTTLE
  • ndc11
    0280608002
    2 BOTTLE in 1 PACKAGE, COMBINATION (0280-6080-02) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE
  • ndc11
    0280608004
    1 BOTTLE, PLASTIC in 1 CARTON (0280-6080-04) / 50 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • ndc11
    0280608016
    160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (0280-6080-16)
  • ndc11
    0280608020
    1 BOTTLE, PLASTIC in 1 CARTON (0280-6080-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • ndc11
    0280608040
    1 BOTTLE, PLASTIC in 1 CARTON (0280-6080-40) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
  • ndc11
    0280608080
    1 BOTTLE, PLASTIC in 1 CARTON (0280-6080-80) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
N021920
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": {
    "590f3be2-20df-4643-9114-e7ed4cf9155c": {
      "match": "brand_token",
      "title": "ALEVE (NAPROXEN SODIUM) TABLET [NAVAJO MANUFACTURING COMPANY INC.]",
      "spl_version": "5",
      "published_date": "2026-04-09"
    }
  },
  "productid": "0280-6080_4526c253-b571-1d84-e063-6394a90ae3f9",
  "productndc": "0280-6080",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "orange_book": {
    "appl_no": "021920",
    "products": [
      {
        "rs": true,
        "rld": true,
        "te_code": null,
        "strength": "EQ 200MG BASE",
        "product_no": "001",
        "approval_date": "Feb 17, 2006"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "NAPROXEN SODIUM",
  "proprietary_name": "Aleve",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA021920",
  "marketing_category": "NDA",
  "nonproprietary_name": "Naproxen Sodium",
  "start_marketing_date": "20070220",
  "active_numerator_strength": "220"
}

Related drugs

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