Phenytoin
- Product NDC
- 17856-0067
- 11-digit product format
- 178560067
- Labeler code
- 17856
- Product ID
- 17856-0067_82c40b58-dc51-435a-9447-e3041bc921b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenytoin
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Atlantic Biologicals Corps
- Application
- ANDA040420
- Marketing category
- ANDA
- Marketing start
- 2002-06-24
- Marketing end
- 0000-00-00
- Substance
- PHENYTOIN
- Active strength
- 125 mg/5mL
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Cytochrome P450 1A2 Inducers [MoA],Cytochrome P450 2B6 Inducers [MoA],Cytochrome P450 2C8 Inducers [MoA],Cytochrome P450 2C19 Inducers [MoA],Cytochrome P450 2D6 Inducers [MoA],Cytochrome P450 3A Inducers [MoA],Cytochrome P450 2C9 Inducers [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-0067-3 | Phenytoin | 4 mL in 1 CUP | SUSPENSION | 4 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0067 | PHENYTOIN SUSPENSION [ATLANTIC BIOLOGICALS CORPS] | 2 | Legacy NDC, 1 package rows | 20120504_25acb26b-04ef-4589-8955-71d777dc813d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17856-0067-3 | 17856006703 | 4 mL in 1 CUP | 4 ml | Historical |