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Risperidone

NDC 63304-950, Risperidone, tablet, orally disintegrating, from Sun Pharmaceutical Industries, Inc..

Product NDC
63304-950
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077542
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63304-950 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RISPERIDONE1 mg/1

Pharmacologic classes

Atypical Antipsychotic [EPC]

Package NDCNDC-11Package
63304-950-0563304095005500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63304-950-05)
63304-950-176330409501710 POUCH in 1 BOX, UNIT-DOSE (63304-950-17) / 1 TABLET, ORALLY DISINTEGRATING in 1 POUCH (63304-950-11)
63304-950-306330409503030 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (63304-950-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f91f551e-926f-440d-83d2-357e9d7484fe

Use it

Look up 63304-950 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-950 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-950. 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.