Divalproex Sodium
- Product NDC
- 50090-4187
- 11-digit product format
- 500904187
- Labeler code
- 50090
- Product ID
- 50090-4187_837d0039-70cd-4aea-bbb6-8fdbb8b2798a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Divalproex Sodium
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090070
- Marketing category
- ANDA
- Marketing start
- 2013-08-11
- Marketing end
- 0000-00-00
- Substance
- DIVALPROEX SODIUM
- Active strength
- 500 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
- 2020-12-31
- 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 |
|---|
| 50090-4187-0 | 50090418700 | 32 BLISTER PACK in 1 CARTON (50090-4187-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 32 blister pack | 2019-03-14 | 0000-00-00 | No | No | Current |