Zonisamide
- Product NDC
- 31722-228
- 11-digit product format
- 317220228
- Labeler code
- 31722
- Product ID
- 31722-228_62729c28-3535-4195-9218-33a9039e4eae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Zonisamide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals
- Application
- ANDA077869
- Marketing category
- ANDA
- Marketing start
- 2012-02-21
- Marketing end
- 0000-00-00
- Substance
- ZONISAMIDE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Decreased Central Nervous System Disorganized Electrical Activity [PE],Anti-epileptic Agent [EPC],Sulfonamides [CS],Carbonic Anhydrase Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 31722-228 | ZONISAMIDE CAPSULE [CAMBER PHARMACEUTICALS] | 1 | Legacy NDC | 20120227_0c160018-e3fb-4f04-9475-c4cf2cceb1b7.zip |