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oxybutynin

NDC 50090-5353, oxybutynin, tablet, film coated, extended release, from A-S Medication Solutions.

Product NDC
50090-5353
Status
Listed
Labeler
A-S Medication Solutions
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202332
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50090-5353 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • OXYBUTYNIN CHLORIDE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
50090-5353-05009053530090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-5353-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1f95920c-5dc2-44e4-b61d-b2c5e05390ba

Use it

Look up 50090-5353 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50090-5353 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50090-5353. 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.