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Diphenoxylate Hydrochloride and Atropine Sulfate

NDC 68788-8090, diphenoxylate hydrochloride and atropine sulfate, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8090
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213413
DEA schedule
CV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8090 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIPHENOXYLATE HYDROCHLORIDE2.5 mg/1
  • ATROPINE SULFATE.025 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
68788-8090-26878880900220 TABLET in 1 BOTTLE (68788-8090-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/46d5b27b-a710-4767-b308-4f673ddb354c

Use it

Look up 68788-8090 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8090 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8090. 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.