Divalproex Sodium is a Oral Tablet, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Contract Pharmacy Services-pa. The primary component is Divalproex Sodium.
Product ID | 67046-146_5a92534c-5787-af98-e053-2991aa0aa8ca |
NDC | 67046-146 |
Product Type | Human Prescription Drug |
Proprietary Name | Divalproex Sodium |
Generic Name | Divalproex Sodium |
Dosage Form | Tablet, Extended Release |
Route of Administration | ORAL |
Marketing Start Date | 2017-10-02 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA090070 |
Labeler Name | Contract Pharmacy Services-PA |
Substance Name | DIVALPROEX SODIUM |
Active Ingredient Strength | 500 mg/1 |
Pharm Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2017-10-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA090070 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090070 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090070 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090070 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090070 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090070 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090070 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-10-02 |
Inactivation Date | 2020-01-31 |
Marketing Category | ANDA |
Application Number | ANDA090070 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2017-10-02 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
DIVALPROEX SODIUM | 500 mg/1 |
SPL SET ID: | 5a92253f-a665-afe2-e053-2991aa0a90cd |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
68001-105 | Divalproex Sodium | Divalproex Sodium |
68001-106 | Divalproex Sodium | Divalproex Sodium |
68071-4102 | Divalproex Sodium | Divalproex Sodium |
68084-313 | divalproex sodium | divalproex sodium |
68084-310 | Divalproex Sodium | Divalproex Sodium |
68084-415 | Divalproex Sodium | Divalproex Sodium |
68084-782 | Divalproex Sodium | Divalproex Sodium |
68084-776 | Divalproex Sodium | Divalproex Sodium |
68151-1164 | Divalproex Sodium | Divalproex Sodium |
68151-4162 | Divalproex Sodium | Divalproex Sodium |
68180-266 | Divalproex Sodium | Divalproex Sodium |
68180-267 | Divalproex Sodium | Divalproex Sodium |
68180-265 | Divalproex Sodium | Divalproex Sodium |
68382-032 | Divalproex Sodium | Divalproex Sodium |
68382-033 | Divalproex Sodium | Divalproex Sodium |
68382-031 | Divalproex Sodium | Divalproex Sodium |
68382-133 | Divalproex Sodium | Divalproex Sodium |
68382-134 | Divalproex Sodium | Divalproex Sodium |
68382-106 | divalproex sodium | divalproex sodium |
68788-7183 | Divalproex Sodium | Divalproex Sodium |
68788-7295 | Divalproex Sodium | Divalproex Sodium |
68788-7177 | Divalproex sodium | Divalproex sodium |
69189-0046 | Divalproex Sodium | Divalproex Sodium |
70518-0282 | Divalproex Sodium | Divalproex Sodium |
70518-0312 | Divalproex Sodium | Divalproex Sodium |
70518-0463 | Divalproex Sodium | Divalproex Sodium |
70518-0613 | Divalproex Sodium | Divalproex Sodium |
70518-0374 | Divalproex Sodium | Divalproex Sodium |
70518-1556 | Divalproex Sodium | Divalproex Sodium |
70518-1661 | Divalproex Sodium | Divalproex Sodium |
70518-1138 | Divalproex Sodium | Divalproex Sodium |
70518-1781 | Divalproex sodium | Divalproex sodium |
70518-1749 | divalproex sodium | divalproex sodium |
70518-1558 | Divalproex Sodium | Divalproex Sodium |
70518-1897 | Divalproex sodium | Divalproex sodium |
0615-1393 | Divalproex sodium | Divalproex sodium |
71335-0008 | Divalproex Sodium | Divalproex Sodium |
71610-205 | Divalproex sodium | Divalproex sodium |
71610-032 | Divalproex Sodium | Divalproex Sodium |
71610-157 | Divalproex sodium | Divalproex sodium |
71610-201 | Divalproex Sodium | Divalproex Sodium |
71610-030 | Divalproex Sodium | Divalproex Sodium |
0615-7532 | Divalproex Sodium | Divalproex Sodium |
0615-7531 | Divalproex Sodium | Divalproex Sodium |
0615-7533 | Divalproex Sodium | Divalproex Sodium |
0615-7554 | Divalproex Sodium | Divalproex Sodium |
71610-031 | Divalproex Sodium | Divalproex Sodium |
0615-7555 | Divalproex Sodium | Divalproex Sodium |
0615-7848 | Divalproex Sodium | Divalproex Sodium |
0615-7950 | Divalproex Sodium | Divalproex Sodium |