50090-4861-0 |
50090-4861 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20200122 |
N/A |
ANDA |
ANDA079163 |
A-S Medication Solutions |
DIVALPROEX SODIUM |
125 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4861-0) |
51655-365-52 |
51655-365 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20200529 |
N/A |
ANDA |
ANDA079163 |
Northwind Pharmaceuticals, LLC |
DIVALPROEX SODIUM |
250 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-365-52) |
70518-2017-2 |
70518-2017 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20230130 |
N/A |
ANDA |
ANDA079163 |
REMEDYREPACK INC. |
DIVALPROEX SODIUM |
125 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2017-2) |
50090-4409-0 |
50090-4409 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20190715 |
N/A |
ANDA |
ANDA079163 |
A-S Medication Solutions |
DIVALPROEX SODIUM |
500 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4409-0) |
55700-938-60 |
55700-938 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20210910 |
N/A |
ANDA |
ANDA079163 |
Quality Care Products, LLC |
DIVALPROEX SODIUM |
250 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55700-938-60) |
55700-939-60 |
55700-939 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20210910 |
N/A |
ANDA |
ANDA079163 |
Quality Care Products, LLC |
DIVALPROEX SODIUM |
500 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55700-939-60) |
71335-2124-1 |
71335-2124 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20220719 |
N/A |
ANDA |
ANDA079163 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
500 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-1) |
71335-2124-2 |
71335-2124 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20220719 |
N/A |
ANDA |
ANDA079163 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
500 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-2) |
71335-2124-3 |
71335-2124 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20220719 |
N/A |
ANDA |
ANDA079163 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
500 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-3) |
71335-0008-4 |
71335-0008 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20211227 |
N/A |
ANDA |
ANDA079163 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
250 mg/1 |
120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-4) |
71335-0008-2 |
71335-0008 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180306 |
N/A |
ANDA |
ANDA079163 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
250 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-2) |
71335-0008-3 |
71335-0008 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180301 |
N/A |
ANDA |
ANDA079163 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
250 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-3) |
71335-0008-1 |
71335-0008 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20181221 |
N/A |
ANDA |
ANDA079163 |
Bryant Ranch Prepack |
DIVALPROEX SODIUM |
250 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-1) |
29300-138-05 |
29300-138 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20111001 |
N/A |
ANDA |
ANDA079163 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
125 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-05) |
29300-139-05 |
29300-139 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20111001 |
N/A |
ANDA |
ANDA079163 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
250 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-05) |
29300-139-10 |
29300-139 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20111001 |
N/A |
ANDA |
ANDA079163 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
250 mg/1 |
1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-10) |
29300-140-01 |
29300-140 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20111001 |
N/A |
ANDA |
ANDA079163 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
500 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-01) |
29300-140-05 |
29300-140 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20111001 |
N/A |
ANDA |
ANDA079163 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
500 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-05) |
29300-140-10 |
29300-140 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20111001 |
N/A |
ANDA |
ANDA079163 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
500 mg/1 |
1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-10) |
29300-138-10 |
29300-138 |
HUMAN PRESCRIPTION DRUG |
Divalproex Sodium |
Divalproex Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20111001 |
N/A |
ANDA |
ANDA079163 |
Unichem Pharmaceuticals (USA), Inc. |
DIVALPROEX SODIUM |
125 mg/1 |
1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-10) |