Valproic
- Product NDC
- 67046-806
- 11-digit product format
- 670460806
- Labeler code
- 67046
- Product ID
- 67046-806_9fbfe4dc-c4df-4911-a440-099c860cb923
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Valproic Acid
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- Application
- ANDA073229
- Marketing category
- ANDA
- Marketing start
- 2010-04-05
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 67046-806-30 | Valproic | 30 in 1 BLISTER PACK | CAPSULE, LIQUID FILLED | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-806 | VALPROIC (VALPROIC ACID) CAPSULE, LIQUID FILLED [CONTRACT PHARMACY SERVICES-PA] | 1 | Legacy NDC, 1 package rows | 20100406_9fbfe4dc-c4df-4911-a440-099c860cb923.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67046-806-30 | 67046080630 | 30 in 1 BLISTER PACK | Historical |