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Guaifenesin and Dextromethorphan HBR

NDC 43598-232, Guaifenesin and Dextromethorphan HBR, tablet, extended release, from Dr. Reddy's Laboratories Inc..

Product NDC
43598-232
Status
Listed
Labeler
Dr. Reddy's Laboratories Inc.
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA217340
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43598-232 \
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Product

Active ingredients and packages

Active ingredients

  • GUAIFENESIN1200 mg/1
  • DEXTROMETHORPHAN HYDROBROMIDE60 mg/1

Pharmacologic classes

Decreased Respiratory Secretion Viscosity [PE]; Expectorant [EPC]; Increased Respiratory Secretions [PE]; 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
43598-232-37435980232373 BLISTER PACK in 1 CARTON (43598-232-37) / 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

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 43598-232 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43598-232 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.