valproic acid
- Product NDC
- 63739-086
- 11-digit product format
- 637390086
- Labeler code
- 63739
- Product ID
- 63739-086_efd12ec8-8f38-c1e3-e053-2995a90a685a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- valproic acid
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- McKesson Corporation dba SKY Packaging
- Application
- ANDA073229
- Marketing category
- ANDA
- Marketing start
- 2021-07-13
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63739-086 | VALPROIC ACID CAPSULE [MCKESSON CORPORATION DBA SKY PACKAGING] | 15 | Legacy NDC | 20250115_c7079e61-bf75-10c9-e053-2995a90a62ed.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63739-086-10 | 63739008610 | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-086-10) > 10 CAPSULE in 1 BLISTER PACK | 10 blister pack | 2021-07-13 | 0000-00-00 | No | No | Current |