NDC 72789-286 – Divalproex sodium
Divalproex Sodium 250 mg/1 · Tablet, Extended Release · Oral
Product NDC72789-286
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- PD-Rx 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 250 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72789-286-60 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-286-60) | Nov 17, 2022 |
Other Divalproex Sodium products
- 65162-757 Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Amneal Pharmaceuticals LLC
- 65162-755 Divalproex Sodium 250 mg/1 · Tablet, Extended Release · Amneal Pharmaceuticals LLC
- 50268-259 Divalproex Sodium 250 mg/1 · Tablet, Extended Release · AvPAK
- 50268-260 Divalproex Sodium 500 mg/1 · Tablet, Extended Release · AvPAK
- 71335-1883 Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Bryant Ranch Prepack
- 55154-2345 Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Cardinal Health 107, LLC
- 67046-2021 Divalproex Sodium 250 mg/1 · Tablet, Extended Release · Coupler LLC
- 68180-260 Divalproex Sodium 250 mg/1 · Tablet, Extended Release · Lupin Pharmaceuticals, Inc.
- 68180-261 Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Lupin Pharmaceuticals, Inc.
- 0904-7182 Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Major Pharmaceuticals
- 0615-8376 Divalproex Sodium 250 mg/1 · Tablet, Extended Release · NCS HealthCare of KY, LLC dba Vangard Labs
- 0615-8377 Divalproex Sodium 500 mg/1 · Tablet, Extended Release · NCS HealthCare of KY, LLC dba Vangard Labs