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Guaifenesin and Codeine Phosphate

NDC 0121-0775, Guaifenesin and Codeine Phosphate, solution, from PAI Holdings, LLC.

Product NDC
0121-0775
Status
Listed
Labeler
PAI Holdings, LLC
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M012
DEA schedule
CV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0775 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GUAIFENESIN100 mg/5mL
  • CODEINE PHOSPHATE10 mg/5mL

Pharmacologic classes

Decreased Respiratory Secretion Viscosity [PE]; Expectorant [EPC]; Full Opioid Agonists [MoA]; Increased Respiratory Secretions [PE]; Opioid Agonist [EPC]

Package NDCNDC-11Package
0121-0775-0400121077504118 mL in 1 BOTTLE (0121-0775-04)
0121-0775-1600121077516473 mL in 1 BOTTLE (0121-0775-16)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 00121077504

    GET /v1/drugs/nadac/00121077504

  • NADAC price for package 00121077516

    GET /v1/drugs/nadac/00121077516

Use it

Look up 0121-0775 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0775 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0121-0775. 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.