VALPROIC ACID
- Product NDC
- 17856-0675
- 11-digit product format
- 178560675
- Labeler code
- 17856
- Product ID
- 17856-0675_be370144-e2b2-497b-8c44-983f9a6dc242
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- VALPROIC ACID
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- ANDA075379
- Marketing category
- ANDA
- Marketing start
- 2019-05-21
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-0675-1 | VALPROIC ACID | 72 in 1 CUP, UNIT-DOSE | SOLUTION | 72 | | 4 |
| 17856-0675-2 | VALPROIC ACID | 5 mL in 1 CUP, UNIT-DOSE | SOLUTION | 5 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-0675 | VALPROIC ACID SOLUTION [ATLANTIC BIOLOGICALS CORP.] | 4 | Legacy NDC, 2 package rows | 20240522_1be5ac3c-9a9d-4b24-88b8-0df28f9a5e8c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17856-0675-1 | 17856067501 | 72 CUP, UNIT-DOSE in 1 CUP, UNIT-DOSE (17856-0675-1) > 5 mL in 1 CUP, UNIT-DOSE (17856-0675-2) | | 2022-07-08 | 0000-00-00 | No | No | Current |
| 17856-0675-2 | 17856067502 | 5 mL in 1 CUP, UNIT-DOSE | 5 ml | | | | | Historical |