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CYPROHEPTADINE HYDROCHLORIDE

NDC 70752-232, CYPROHEPTADINE HYDROCHLORIDE, tablet, from Quagen Pharmaceuticals, LLC.

Product NDC
70752-232
Status
Listed
Labeler
Quagen Pharmaceuticals, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212491
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70752-232 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CYPROHEPTADINE HYDROCHLORIDE2 mg/1
Package NDCNDC-11Package
70752-232-037075202320330 TABLET in 1 BOTTLE (70752-232-03)
70752-232-057075202320560 TABLET in 1 BOTTLE (70752-232-05)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e6d91eae-db29-4e62-89da-1ad764de7ae1

Use it

Look up 70752-232 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70752-232 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70752-232. 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.