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Oxybutynin Chloride

NDC 43063-851, Oxybutynin Chloride, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-851
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209335
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43063-851 \
  -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
43063-851-0143063085101100 TABLET in 1 BOTTLE, PLASTIC (43063-851-01)
43063-851-604306308516060 TABLET in 1 BOTTLE, PLASTIC (43063-851-60)
43063-851-904306308519090 TABLET in 1 BOTTLE, PLASTIC (43063-851-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0c021aad-97a3-4404-a11e-cdd2ec731c6b

Use it

Look up 43063-851 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-851 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-851. 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.