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Hydrocodone Bitartrate and Acetaminophen

NDC 10702-192, Hydrocodone Bitartrate and Acetaminophen, tablet, from KVK-Tech, Inc..

Product NDC
10702-192
Status
Listed
Labeler
KVK-Tech, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209036
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10702-192 \
  -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
10702-192-0110702019201100 TABLET in 1 BOTTLE (10702-192-01)
10702-192-031070201920330 TABLET in 1 BOTTLE (10702-192-03)
10702-192-10107020192101000 TABLET in 1 BOTTLE (10702-192-10)
10702-192-5010702019250500 TABLET in 1 BOTTLE (10702-192-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f1063950-b302-4898-81c2-b1626c9c16ef

  • NADAC price for package 10702019201

    GET /v1/drugs/nadac/10702019201

Use it

Look up 10702-192 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10702-192 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10702-192. 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.