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Hydrocodone Bitartrate and Acetaminophen

NDC 43386-358, Hydrocodone Bitartrate and Acetaminophen, tablet, from Lupin Pharmaceuticals,Inc..

Product NDC
43386-358
Status
Listed
Labeler
Lupin Pharmaceuticals,Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206245
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43386-358 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCODONE BITARTRATE10 mg/1
  • ACETAMINOPHEN325 mg/1

Pharmacologic classes

Opioid Agonist [EPC]; Opioid Agonists [MoA]

Package NDCNDC-11Package
43386-358-0143386035801100 TABLET in 1 BOTTLE (43386-358-01)
43386-358-0543386035805500 TABLET in 1 BOTTLE (43386-358-05)
43386-358-10433860358101000 TABLET in 1 BOTTLE (43386-358-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/26a2178e-e0e5-4d61-81fd-e30a3142f1f2

Use it

Look up 43386-358 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43386-358 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43386-358. 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.