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Oxybutynin Chloride

NDC 83939-0022, Oxybutynin Chloride, tablet, from VERITYRX, LLC.

Product NDC
83939-0022
Status
Listed
Labeler
VERITYRX, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209823
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/83939-0022 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYBUTYNIN CHLORIDE5 mg/1

Pharmacologic classes

Cholinergic Muscarinic Antagonist [EPC]; Cholinergic Muscarinic Antagonists [MoA]

Package NDCNDC-11Package
83939-0022-1839390022011 TABLET in 1 POUCH (83939-0022-1)
83939-0022-28393900220250 POUCH in 1 BOX, UNIT-DOSE (83939-0022-2) / 1 TABLET in 1 POUCH
83939-0022-383939002203100 POUCH in 1 BOX, UNIT-DOSE (83939-0022-3) / 1 TABLET in 1 POUCH

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/427b6ffb-3ff4-932f-e063-6394a90ae8b9

Use it

Look up 83939-0022 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/83939-0022 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 83939-0022. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.