Zanaflex
- Product NDC
- 10144-602
- 11-digit product format
- 101440602
- Labeler code
- 10144
- Product ID
- 10144-602_7897aa33-13b7-f553-e053-2a91aa0a2c3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tizanidine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Acorda Therapeutics, Inc.
- Application
- NDA021447
- Marketing category
- NDA
- Marketing start
- 2005-04-04
- Marketing end
- 2019-07-31
- Substance
- TIZANIDINE HYDROCHLORIDE
- Active strength
- 2 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