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BETAXOLOL HYDROCHLORIDE

NDC 10702-014, betaxolol hydrochloride, tablet, coated, from KVK-TECH, INC..

Product NDC
10702-014
Status
Listed
Labeler
KVK-TECH, INC.
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078962
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10702-014 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BETAXOLOL HYDROCHLORIDE20 mg/1

Pharmacologic classes

Adrenergic beta-Antagonists [MoA]; beta-Adrenergic Blocker [EPC]

Package NDCNDC-11Package
10702-014-0110702001401100 TABLET, COATED in 1 BOTTLE (10702-014-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f3b50bbb-df03-4ed7-9d8d-180edc2abd54

  • NADAC price for package 10702001401

    GET /v1/drugs/nadac/10702001401

Use it

Look up 10702-014 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10702-014 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10702-014. 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.