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Hydrocodone Bitartrate and Acetaminophen

NDC 0121-4772, HYDROCODONE BITARTRATE and ACETAMINOPHEN, solution, from PAI Holdings, LLC dba PAI Pharma.

Product NDC
0121-4772
Status
Listed
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040838
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0121-4772 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCODONE BITARTRATE2.5 mg/5mL
  • ACETAMINOPHEN108 mg/5mL

Pharmacologic classes

Opioid Agonist [EPC]; Opioid Agonists [MoA]

Package NDCNDC-11Package
0121-4772-40001214772404 TRAY in 1 CASE (0121-4772-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-4772-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c29b97e9-8097-4d87-a420-ccf5aec8274a

Use it

Look up 0121-4772 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0121-4772 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0121-4772. 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.