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Guaifenesin and Codeine Phosphate

NDC 0121-1550, Guaifenesin and Codeine Phosphate, solution, from PAI Holdings, LLC.

Product NDC
0121-1550
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/0121-1550 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GUAIFENESIN200 mg/10mL
  • CODEINE PHOSPHATE20 mg/10mL

Pharmacologic classes

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

Package NDCNDC-11Package
0121-1550-000012115500010 TRAY in 1 CASE (0121-1550-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1550-10)
0121-1550-40001211550404 TRAY in 1 CASE (0121-1550-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0121-1550-10)

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 0121-1550 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0121-1550 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0121-1550. 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.