Tizanidine
- Product NDC
- 51079-998
- 11-digit product format
- 510790998
- Labeler code
- 51079
- Product ID
- 51079-998_7d8e5f3c-a36f-d657-e053-2a91aa0a2140
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- tizanidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA076354
- Marketing category
- ANDA
- Marketing start
- 2003-06-15
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record