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hydrocodone bitartrate and acetaminophen

NDC 71930-043, hydrocodone bitartrate and acetaminophen, tablet, from Eywa Pharma Inc.

Product NDC
71930-043
Status
Listed
Labeler
Eywa Pharma Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207509
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71930-043 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCODONE BITARTRATE7.5 mg/1
  • ACETAMINOPHEN300 mg/1

Pharmacologic classes

Opioid Agonist [EPC]; Opioid Agonists [MoA]

Package NDCNDC-11Package
71930-043-1271930004312100 TABLET in 1 BOTTLE (71930-043-12)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8a201e19-3e47-7e58-e053-2995a90ab1d5

Use it

Look up 71930-043 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71930-043 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71930-043. 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.