valproic acid
- Product NDC
- 70518-0730
- 11-digit product format
- 705180730
- Labeler code
- 70518
- Product ID
- 70518-0730_e21ed5f6-4077-0857-e053-2995a90a0a7c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- valproic acid
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA073229
- Marketing category
- ANDA
- Marketing start
- 2017-09-11
- 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 |
|---|
| 70518-0730 | VALPROIC ACID CAPSULE [REMEDYREPACK INC.] | 11 | Legacy NDC | 20250523_b7872509-f197-4e7a-8248-7dd6d376e408.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0730-0 | 70518073000 | 30 CAPSULE in 1 BLISTER PACK (70518-0730-0) | 30 capsule | 2017-09-11 | 0000-00-00 | No | No | Current |
| 70518-0730-1 | 70518073001 | 100 POUCH in 1 BOX (70518-0730-1) > 1 CAPSULE in 1 POUCH (70518-0730-2) | 100 pouch | 2022-01-19 | 0000-00-00 | No | No | Current |