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Promethazine Hydrochloride

NDC 76420-389, Promethazine Hydrochloride, suppository, from Asclemed USA, Inc..

Product NDC
76420-389
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
SUPPOSITORY
Route
RECTAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040500
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-389 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROMETHAZINE HYDROCHLORIDE25 mg/1

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]

Package NDCNDC-11Package
76420-389-307642003893012 BLISTER PACK in 1 CARTON (76420-389-30) / 1 SUPPOSITORY in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1b1cee64-c0b5-4da6-92d0-1769350a5181

Use it

Look up 76420-389 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-389 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-389. 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.