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Hydrocodone Bitartrate and Acetaminophen

NDC 10702-193, Hydrocodone Bitartrate and Acetaminophen, tablet, from KVK-Tech, Inc..

Product NDC
10702-193
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/10702-193 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • HYDROCODONE BITARTRATE7.5 mg/1
  • ACETAMINOPHEN300 mg/1

Pharmacologic classes

Opioid Agonist [EPC]; Opioid Agonists [MoA]

Package NDCNDC-11Package
10702-193-0110702019301100 TABLET in 1 BOTTLE (10702-193-01)
10702-193-031070201930330 TABLET in 1 BOTTLE (10702-193-03)
10702-193-10107020193101000 TABLET in 1 BOTTLE (10702-193-10)
10702-193-5010702019350500 TABLET in 1 BOTTLE (10702-193-50)

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 10702019301

    GET /v1/drugs/nadac/10702019301

Use it

Look up 10702-193 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10702-193 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10702-193. 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.