Zanaflex
- Product NDC
- 10144-594
- 11-digit product format
- 101440594
- Labeler code
- 10144
- Product ID
- 10144-594_7897aa33-13b7-f553-e053-2a91aa0a2c3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tizanidine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Acorda Therapeutics, Inc.
- Application
- NDA020397
- Marketing category
- NDA
- Marketing start
- 1997-01-01
- Marketing end
- 2020-09-30
- Substance
- TIZANIDINE HYDROCHLORIDE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record