Valproic
- Product NDC
- 17856-4012
- 11-digit product format
- 178564012
- Labeler code
- 17856
- Product ID
- 17856-4012_c083ff59-eb2c-46d0-8be0-b19d11776c09
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valproic Acid
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- 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
- 2021-12-31
- 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 |
|---|
| 17856-4012-1 | Valproic | 1 in 1 POUCH | CAPSULE, LIQUID FILLED | 1 | | 1 |
| 17856-4012-1 | Valproic | 100 in 1 BOX, UNIT-DOSE | CAPSULE, LIQUID FILLED | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-4012 | VALPROIC (VALPROIC ACID) CAPSULE, LIQUID FILLED [ATLANTIC BIOLOGICALS CORP.] | 1 | Legacy NDC, 2 package rows | 20200827_86dd50d5-4890-4b3c-8681-18796eff97b6.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 |
|---|
| 17856-4012-1 | 17856401201 | 100 POUCH in 1 BOX, UNIT-DOSE (17856-4012-1) > 1 CAPSULE, LIQUID FILLED in 1 POUCH | 100 pouch | 2020-08-26 | 0000-00-00 | No | No | Current |