Valproic
- Product NDC
- 42291-844
- 11-digit product format
- 422910844
- Labeler code
- 42291
- Product ID
- 42291-844_d5ca21ed-a3ee-b7dd-e053-2a95a90ac112
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valproic Acid
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA073229
- Marketing category
- ANDA
- Marketing start
- 2018-05-29
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-844-01 | 42291084401 | 100 CAPSULE, LIQUID FILLED in 1 BOTTLE (42291-844-01) | 2018-05-29 | 0000-00-00 | No | No | Current |