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Hydrocodone Bitartrate and Acetaminophen

NDC 63304-497, Hydrocodone Bitartrate and Acetaminophen, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
63304-497
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040826
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63304-497 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ACETAMINOPHEN325 mg/1
  • HYDROCODONE BITARTRATE10 mg/1

Pharmacologic classes

Opioid Agonist [EPC]; Opioid Agonists [MoA]

Package NDCNDC-11Package
63304-497-0163304049701100 TABLET in 1 BOTTLE (63304-497-01)
63304-497-036330404970310 TABLET in 1 BOTTLE (63304-497-03)
63304-497-0563304049705500 TABLET in 1 BOTTLE (63304-497-05)
63304-497-10633040497101000 TABLET in 1 BOTTLE (63304-497-10)
63304-497-696330404976910 BLISTER PACK in 1 CARTON (63304-497-69) / 1 TABLET in 1 BLISTER PACK (63304-497-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6e153073-ca78-481e-9e9c-0365ee3f3d59

Use it

Look up 63304-497 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63304-497 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63304-497. 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.