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tizanidine

NDC 70771-1335, tizanidine, tablet, from Zydus Lifesciences Limited.

Product NDC
70771-1335
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208187
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1335 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TIZANIDINE HYDROCHLORIDE2 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
70771-1335-0707711335001000 TABLET in 1 BOTTLE (70771-1335-0)
70771-1335-37077113350330 TABLET in 1 BOTTLE (70771-1335-3)
70771-1335-47077113350410 BLISTER PACK in 1 CARTON (70771-1335-4) / 10 TABLET in 1 BLISTER PACK (70771-1335-2)
70771-1335-870771133508150 TABLET in 1 BOTTLE (70771-1335-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/89105a78-badb-469e-966e-195fa3a53f0a

Use it

Look up 70771-1335 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1335 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1335. 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.