Valproic Acid
- Product NDC
- 55154-1575
- 11-digit product format
- 551541575
- Labeler code
- 55154
- Product ID
- 55154-1575_422805a2-6aae-47b1-bdda-4b8b8684a333
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valproic Acid
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA070868
- Marketing category
- ANDA
- Marketing start
- 2003-12-10
- Marketing end
- 0000-00-00
- Substance
- VALPROIC ACID
- Active strength
- 250 mg/5mL
- Pharmacologic classes
- Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record