OXYBUTYNIN BASE

NDC product · U.S. Food and Drug Administration (openFDA) · United States

Product NDC 49169-1013
Package NDC 49169-1013-0
SPL ID f18713f1-63b8-059e-e053-2995a90ac3e4

What the source publishes

Labeler: PCAS FRANCE
Active ingredients: OXYBUTYNIN BASE
Form: POWDER
Administrative status: present-in-source-snapshot
Marketing status: BULK INGREDIENT
Product type: BULK INGREDIENT

Names this record is found by

Complete source data

us:fda:ndc:49169-1013_f18713f1-63b8-059e-e053-2995a90ac3e4

{
  "name": "OXYBUTYNIN BASE",
  "splId": "f18713f1-63b8-059e-e053-2995a90ac3e4",
  "labels": [],
  "routes": [],
  "labeler": "PCAS FRANCE",
  "finished": false,
  "packaging": [
    {
      "description": "25 kg in 1 DRUM (49169-1013-0)",
      "package_ndc": "49169-1013-0",
      "identifierStatus": "well-formed",
      "marketing_start_date": "14-AUG-09"
    }
  ],
  "productId": "49169-1013_f18713f1-63b8-059e-e053-2995a90ac3e4",
  "useDomain": "unknown",
  "dosageForm": "POWDER",
  "productNdc": "49169-1013",
  "deaSchedule": null,
  "genericName": "OXYBUTYNIN BASE",
  "productType": "BULK INGREDIENT",
  "listingStatus": "present-in-source-snapshot",
  "targetSpecies": [],
  "approvalStatus": "not-established-by-ndc-listing",
  "labelAssociation": "openFDA-harmonized-set-ids; not a product-level approval match",
  "marketingEndDate": null,
  "activeIngredients": [
    {
      "name": "OXYBUTYNIN",
      "strength": "1 kg/kg"
    }
  ],
  "applicationNumber": null,
  "marketingCategory": "BULK INGREDIENT",
  "stateRestrictions": {
    "status": "not-collected",
    "observations": []
  },
  "useDomainEvidence": {
    "basis": "unreviewed",
    "field": null,
    "value": null,
    "version": 1,
    "sourceId": "us.fda.ndc"
  },
  "marketingStartDate": "20090814",
  "targetSpeciesStatus": "not-reported",
  "prescriptionCategory": "unknown",
  "harmonizedIdentifiers": {},
  "listingExpirationDate": "20261231"
}

NDC Directory

U.S. Food and Drug Administration / openFDA

Retrieved: November 15, 2026
Licence: CC0 1.0
Source id: us.fda.ndc

Official source

What this source does not establish

Complete published endpoint, not a claim that FDA lists every medicine used in the US.
NDC listing, marketing category and application-number assertions are not proof of approval.
Tentative approval, discontinued products and historical submissions remain distinct.
Official document links only; linked documents have not been relicensed or mirrored.
No state restrictions, individual eligibility, or prescribing recommendations inferred.
UNII and RxNorm identifiers are source-asserted openFDA harmonization at record scope; arrays do not pair identifiers to individual products or ingredients, and are not GSID/PhPID or substitution evidence.

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