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Diphenoxylate Hydrochloride and Atropine Sulfate

NDC 70518-3915, diphenoxylate hydrochloride and atropine sulfate, tablet, from REMEDYREPACK INC..

Product NDC
70518-3915
Status
Listed
Labeler
REMEDYREPACK 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/70518-3915 \
  -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
70518-3915-17051839150130 TABLET in 1 BLISTER PACK (70518-3915-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3d0e2877-7a74-433f-8a31-e3e54aa9dc9f

Use it

Look up 70518-3915 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-3915 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-3915. 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.