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Hydrocodone Bitartrate and Acetaminophen

NDC 76420-215, Hydrocodone Bitartrate and Acetaminophen, tablet, from Asclemed USA, Inc..

Product NDC
76420-215
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202991
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-215 \
  -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
76420-215-0176420021501100 TABLET in 1 BOTTLE (76420-215-01)
76420-215-307642002153030 TABLET in 1 BOTTLE (76420-215-30)
76420-215-607642002156060 TABLET in 1 BOTTLE (76420-215-60)
76420-215-907642002159090 TABLET in 1 BOTTLE (76420-215-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5c00f98f-dcab-4bdb-901e-02eb873dea31

Use it

Look up 76420-215 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-215 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-215. 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.