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Tizanidine

NDC 70518-0133, Tizanidine, tablet, from REMEDYREPACK INC..

Product NDC
70518-0133
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076286
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0133 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TIZANIDINE HYDROCHLORIDE4 mg/1

Pharmacologic classes

Adrenergic alpha2-Agonists [MoA]; Central alpha-2 Adrenergic Agonist [EPC]

Package NDCNDC-11Package
70518-0133-07051801330060 TABLET in 1 BOTTLE (70518-0133-0)
70518-0133-17051801330190 TABLET in 1 BOTTLE, PLASTIC (70518-0133-1)
70518-0133-37051801330330 TABLET in 1 BOTTLE, PLASTIC (70518-0133-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/59084f59-9a9b-49f0-a9f4-27f3eab9a228

Use it

Look up 70518-0133 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-0133 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-0133. 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.