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Promethazine Hydrochloride

NDC 68382-042, Promethazine Hydrochloride, tablet, from Zydus Pharmaceuticals USA Inc..

Product NDC
68382-042
Status
Listed
Labeler
Zydus Pharmaceuticals 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/68382-042 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROMETHAZINE HYDROCHLORIDE50 mg/1

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]

Package NDCNDC-11Package
68382-042-0168382004201100 TABLET in 1 BOTTLE (68382-042-01)
68382-042-0568382004205500 TABLET in 1 BOTTLE (68382-042-05)
68382-042-10683820042101000 TABLET in 1 BOTTLE (68382-042-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c0c0d4f0-8396-485b-a585-71df01491f6f

  • NADAC price for package 68382004201

    GET /v1/drugs/nadac/68382004201

Use it

Look up 68382-042 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-042 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-042. 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.