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Promethazine Hydrochloride and Dextromethorphan Hydrobromide

NDC 76420-335, Promethazine Hydrochloride and Dextromethorphan Hydrobromide, solution, from Asclemed USA, Inc..

Product NDC
76420-335
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA011265
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-335 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROMETHAZINE HYDROCHLORIDE6.25 mg/5mL
  • DEXTROMETHORPHAN HYDROBROMIDE15 mg/5mL

Pharmacologic classes

Phenothiazine [EPC]; Phenothiazines [CS]; Sigma-1 Agonist [EPC]; Sigma-1 Receptor Agonists [MoA]; Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]; Uncompetitive NMDA Receptor Antagonists [MoA]

Package NDCNDC-11Package
76420-335-0476420033504118 mL in 1 BOTTLE (76420-335-04)
76420-335-1676420033516473 mL in 1 BOTTLE (76420-335-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/702eb7c0-db4c-4729-b69e-99f64c63c7bd

Use it

Look up 76420-335 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-335 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-335. 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.