Valproic
- Product NDC
- 70518-2215
- 11-digit product format
- 705182215
- Labeler code
- 70518
- Product ID
- 70518-2215_8e3b7aa2-cda4-fb45-e053-2a95a90a5c76
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valproic Acid
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA073229
- Marketing category
- ANDA
- Marketing start
- 2019-07-14
- Marketing end
- 0000-00-00
- Substance
- VALPROIC ACID
- Active strength
- 250 mg/1
- 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