Phenytoin 125 mg/5mL
Phenytoin · SUSPENSION · Sun Pharmaceutical Industries, Inc.
No Recall History
Plain English
Phenytoin is a suspension containing phenytoin at 125 mg/5mL, taken oral. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Phenytoin
- Generic Name
- Phenytoin
- NDC Code (Product)
51672-4069- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 125 mg/5mL
- Dosage Form
- SUSPENSION
- Route
- ORAL
- Marketing Status
- Application #
- ANDA040521
- Drug Class
- Anti-epileptic Agent [EPC]
- Marketing Start
- 04/08/2004
Recall History
No Recall HistoryFrequently Asked Questions
What is Phenytoin used for?
Phenytoin contains Phenytoin. It is a suspension taken oral. Consult your doctor for specific uses.
Is Phenytoin a controlled substance?
Phenytoin is not classified as a controlled substance by the DEA.
What is the generic name for Phenytoin?
The generic name for Phenytoin is Phenytoin. There are 9 other brand versions of Phenytoin.
What is the NDC code for Phenytoin 125 mg/5mL?
The NDC (National Drug Code) for Phenytoin 125 mg/5mL is 51672-4069, listed by Sun Pharmaceutical Industries, Inc..
Other Phenytoin Dosages
Other Phenytoin Brands
See all →- Extended Phenytoin Sodium100 mg/10615-8556
- Dilantin Infatabs50 mg/10071-0007
- Phenytoin Sodium100 mg/129300-379
- Phenytoin Sodium100 mg/150090-5700
- Phenytoin Sodium100 mg/151407-982
- PHENYTOIN SODIUM50 mg/mL42192-614
- Phenytoin Sodium100 mg/157664-808
- phenytoin sodium300 mg/162756-432
- Extended Phenytoin Sodium100 mg/165862-692
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)