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Senna-S

NDC 63561-0187, DOCUSATE SODIUM, SENNOSIDES, tablet, film coated, from Granulation Technology, Inc..

Product NDC
63561-0187
Status
Listed
Labeler
Granulation Technology, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
505G(a)(3)
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0187 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SENNOSIDES8.6 mg/1
  • DOCUSATE SODIUM50 mg/1
Package NDCNDC-11Package
63561-0187-163561018701100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-1)
63561-0187-263561018702220 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-2)
63561-0187-3635610187031000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 63561-0187 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0187 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63561-0187. 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.