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ACETAMINOPHEN AND CODEINE PHOSPHATE

NDC 68788-7835, acetaminophen and codeine phosphate, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-7835
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040419
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7835 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN300 mg/1
  • CODEINE PHOSPHATE30 mg/1

Pharmacologic classes

Full Opioid Agonists [MoA]; Opioid Agonist [EPC]

Package NDCNDC-11Package
68788-7835-16878878350115 TABLET in 1 BOTTLE (68788-7835-1)
68788-7835-26878878350220 TABLET in 1 BOTTLE (68788-7835-2)
68788-7835-36878878350330 TABLET in 1 BOTTLE (68788-7835-3)
68788-7835-66878878350660 TABLET in 1 BOTTLE (68788-7835-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2453d635-989d-4569-96b3-4efaf61cca71

Use it

Look up 68788-7835 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-7835 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-7835. 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.