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TRIPROLIDINE HYDROCHLORIDE

NDC 69367-450, TRIPROLIDINE HYDROCHLORIDE, syrup, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-450
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
SYRUP
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M012
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-450 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRIPROLIDINE HYDROCHLORIDE1.25 mg/mL
Package NDCNDC-11Package
69367-450-30693670450301 BOTTLE in 1 CARTON (69367-450-30) / 30 mL in 1 BOTTLE

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 69367-450 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-450 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-450. 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.