Divalproex sodium
- Product NDC
- 60687-654
- 11-digit product format
- 606870654
- Labeler code
- 60687
- Product ID
- 60687-654_e32c073d-ba94-25c1-e053-2a95a90acc01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex sodium
- Dosage form
- CAPSULE, COATED PELLETS
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA213181
- Marketing category
- ANDA
- Marketing start
- 2022-06-28
- Marketing end
- 0000-00-00
- Substance
- DIVALPROEX SODIUM
- Active strength
- 125 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-654-01 | 60687065401 | 100 BLISTER PACK in 1 CARTON (60687-654-01) > 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (60687-654-11) | 100 blister pack | 2022-06-28 | 0000-00-00 | No | No | Current |