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Stimulant Laxative Plus Stool Softener

NDC 68788-7674, Docusate Sodium 50 mg and Sennosides 8.6 mg, tablet, film coated, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-7674
Status
Listed
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
part334
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7674 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SENNOSIDES8.6 mg/1
  • DOCUSATE SODIUM50 mg/1
Package NDCNDC-11Package
68788-7674-168788767401100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7674-1)
68788-7674-66878876740660 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7674-6)

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 68788-7674 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7674 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-7674. 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.