Valproic Acid
- Product NDC
- 68094-193
- 11-digit product format
- 680940193
- Labeler code
- 68094
- Product ID
- 68094-193_2a301501-7348-4640-b5db-bf11f3e4d49e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valproic Acid
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Precision Dose Inc.
- Application
- ANDA070868
- Marketing category
- ANDA
- Marketing start
- 2003-12-10
- Marketing end
- 2023-12-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68094-193-61 | 68094019361 | 10 TRAY in 1 CASE (68094-193-61) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-193-59) | 10 tray | 2003-12-10 | 2023-12-31 | No | No | Current |
| 68094-193-62 | 68094019362 | 3 TRAY in 1 CASE (68094-193-62) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE (68094-193-59) | 3 tray | 2003-12-10 | 2023-12-31 | No | No | Current |