NDC 0378-0472 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC0378-0472
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex sodium
- Labeler
- Mylan Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077567
- Marketed since
- January 29, 2009
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 250 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0378-0472-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0472-01) | Jan 29, 2009 |
| 0378-0472-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0472-05) | Jan 29, 2009 |
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