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Solifenacin succinate

NDC 72303-0832, solifenacin succinate, tablet, film coated, from HEC Pharm USA Inc..

Product NDC
72303-0832
Status
Listed
Labeler
HEC Pharm USA Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213346
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72303-0832 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SOLIFENACIN SUCCINATE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72303-0832-17230308320130 TABLET, FILM COATED in 1 BOTTLE (72303-0832-1)
72303-0832-27230308320290 TABLET, FILM COATED in 1 BOTTLE (72303-0832-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/56026679-4002-a6c6-e063-6294a90a7b55

Use it

Look up 72303-0832 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72303-0832 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72303-0832. 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.