Valproic
- Product NDC
- 63629-7597
- 11-digit product format
- 636297597
- Labeler code
- 63629
- Product ID
- 63629-7597_50589659-3681-497d-91f2-cb0f1e9e294c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valproic Acid
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA073229
- Marketing category
- ANDA
- Marketing start
- 2009-09-08
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-7597 | VALPROIC (VALPROIC ACID) CAPSULE, LIQUID FILLED [BRYANT RANCH PREPACK] | 4 | Legacy NDC | 20220118_50589659-3681-497d-91f2-cb0f1e9e294c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7597-1 | 63629759701 | 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (63629-7597-1) | 2010-03-30 | 0000-00-00 | No | No | Current |