NDC 68180-261 – Divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Oral
Product NDC68180-261
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA209286
- Marketed since
- September 18, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 500 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68180-261-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-01) | Sep 18, 2020 |
| 68180-261-02 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-261-02) | Sep 18, 2020 |
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