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Banophen

NDC 83112-555, Diphenhydramine HCl, tablet, film coated, from Health Department, Oklahoma State.

Product NDC
83112-555
Status
Listed
Labeler
Health Department, Oklahoma State
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/83112-555 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DIPHENHYDRAMINE HYDROCHLORIDE25 mg/1

Pharmacologic classes

Histamine H1 Receptor Antagonists [MoA]; Histamine-1 Receptor Antagonist [EPC]

Package NDCNDC-11Package
83112-555-59831120555591 TABLET, FILM COATED in 1 PACKET (83112-555-59)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2cdbe7df-4c67-9b05-e063-6394a90a4699

Use it

Look up 83112-555 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/83112-555 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 83112-555. 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.