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Oxybutynin Chloride Extended Release

NDC 82804-095, Oxybutynin Chloride, tablet, extended release, from Proficient Rx LP.

Product NDC
82804-095
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206121
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82804-095 \
  -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
82804-095-308280400953030 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-095-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7d2332b4-9e48-4bb2-a2c3-75e16e1d455b

Use it

Look up 82804-095 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-095 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-095. 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.