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oxybutynin chloride

NDC 72789-049, oxybutynin chloride, tablet, extended release, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-049
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207138
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-049 \
  -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
72789-049-907278900499090 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-049-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a1f8be75-2eb9-4eef-8fb4-144ef2bf7ae1

Use it

Look up 72789-049 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-049 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-049. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.