VALPROIC ACID
- Product NDC
- 70518-1968
- 11-digit product format
- 705181968
- Labeler code
- 70518
- Product ID
- 70518-1968_848f5bd5-3329-54f7-e053-2a91aa0a0b05
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VALPROIC ACID
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075379
- Marketing category
- ANDA
- Marketing start
- 2019-03-20
- 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
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record