divalproex sodium - divalproex sodium
Navigation: NDC > Supplier starting with: N > NORTHSTAR RX LLC| Field | Value |
|---|---|
| NDC Code: | 16714-512 |
| Proprietary Name: | divalproex sodium |
| Suffix: | |
| Non-Proprietary Name: | divalproex sodium |
| Dosage Form: | TABLET, DELAYED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 14-07-2009 |
| End of Marketing: | 31-08-2014 |
| Category Name: | ANDA |
| Application Number: | ANDA078853 |
| Labeler: | NORTHSTAR RX LLC |
| Substance Name: | DIVALPROEX SODIUM |
| Active Numerator Strength: | 250 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
| DEA Schedule: |