Divalproex Sodium
- Product NDC
- 43063-295
- 11-digit product format
- 430630295
- Labeler code
- 43063
- Product ID
- 43063-295_a8d5e13f-d6f2-be12-e053-2995a90a0f74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078445
- Marketing category
- ANDA
- Marketing start
- 2009-08-04
- Marketing end
- 0000-00-00
- Substance
- DIVALPROEX SODIUM
- Active strength
- 500 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-295-30 | 43063029530 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-295-30) | 2009-08-31 | 0000-00-00 | No | No | Current |