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Promethazine Hydrochloride

NDC 76420-679, Promethazine Hydrochloride, tablet, from Asclemed USA, Inc..

Product NDC
76420-679
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040596
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-679 \
  -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
76420-679-0176420067901100 TABLET in 1 BOTTLE (76420-679-01)
76420-679-307642006793030 TABLET in 1 BOTTLE (76420-679-30)
76420-679-607642006796060 TABLET in 1 BOTTLE (76420-679-60)
76420-679-907642006799090 TABLET in 1 BOTTLE (76420-679-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b4985d9d-1aa0-4b36-bc98-6a5410ad9bad

Use it

Look up 76420-679 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-679 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-679. 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.