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United States · US · US:65862-945_29ed39d7-180a-93e4-e063-6294a90a73a9

Levalbuterol

Orange BookUNIISPL

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

Identification

ManufacturerAurobindo Pharma Limited
CountryUS (United States)
ATC code
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    6586294525
    5 POUCH in 1 CARTON (65862-945-25) / 5 VIAL, SINGLE-DOSE in 1 POUCH (65862-945-05) / 3 mL in 1 VIAL, SINGLE-DOSE

Annotations

UNII (FDA Substance ID)
WDQ1526QJM
LEVALBUTEROL HYDROCHLORIDE
RxCUI 237160
Orange Book
A207625
ANANAN
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "WDQ1526QJM",
    "rxcui": "237160",
    "inchikey": "OWNWYCOLFIFTLK-YDALLXLXSA-N",
    "display_name": "LEVALBUTEROL HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "RESPIRATORY (INHALATION)",
  "spl_meta": {
    "d6998949-e1cb-4c86-a480-c0dfd9cb75b5": {
      "match": "brand_token",
      "title": "LEVALBUTEROL (LEVALBUTEROL HYDROCHLORIDE) SOLUTION [RITEDOSE PHARMACEUTICALS, LLC]",
      "spl_version": "22",
      "published_date": "2025-12-12"
    }
  },
  "productid": "65862-945_29ed39d7-180a-93e4-e063-6294a90a73a9",
  "productndc": "65862-945",
  "dosage_form": "SOLUTION",
  "orange_book": {
    "appl_no": "207625",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AN",
        "strength": "EQ 0.0103% BASE",
        "product_no": "001",
        "approval_date": "Dec 30, 2016"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AN",
        "strength": "EQ 0.021% BASE",
        "product_no": "002",
        "approval_date": "Dec 30, 2016"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AN",
        "strength": "EQ 0.042% BASE",
        "product_no": "003",
        "approval_date": "Dec 30, 2016"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LEVALBUTEROL HYDROCHLORIDE",
  "proprietary_name": "Levalbuterol",
  "active_ingred_unit": "mg/3mL",
  "application_number": "ANDA207625",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Levalbuterol",
  "start_marketing_date": "20161230",
  "active_numerator_strength": "1.25"
}

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