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Hydrocodone Bitartrate and Acetaminophen

NDC 43386-351, Hydrocodone Bitartrate and Acetaminophen, tablet, from Lupin Pharmaceuticals,Inc..

Product NDC
43386-351
Status
Listed
Labeler
Lupin Pharmaceuticals,Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206142
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43386-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCODONE BITARTRATE5 mg/1
  • ACETAMINOPHEN300 mg/1

Pharmacologic classes

Opioid Agonist [EPC]; Opioid Agonists [MoA]

Package NDCNDC-11Package
43386-351-0143386035101100 TABLET in 1 BOTTLE (43386-351-01)
43386-351-0543386035105500 TABLET in 1 BOTTLE (43386-351-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/48cc1378-ffab-4645-95bb-a05d78066575

Use it

Look up 43386-351 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43386-351 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43386-351. 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.