Product NDC: | 0179-0016 |
Proprietary Name: | Omeprazole |
Non Proprietary Name: | Omeprazole |
Active Ingredient(s): | 40 mg/1 & nbsp; Omeprazole |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, DELAYED RELEASE PELLETS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0179-0016 |
Labeler Name: | KAISER FOUNDATION HOSPITALS |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075347 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090801 |
Package NDC: | 0179-0016-70 |
Package Description: | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOX, UNIT-DOSE (0179-0016-70) |
NDC Code | 0179-0016-70 |
Proprietary Name | Omeprazole |
Package Description | 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOX, UNIT-DOSE (0179-0016-70) |
Product NDC | 0179-0016 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Omeprazole |
Dosage Form Name | CAPSULE, DELAYED RELEASE PELLETS |
Route Name | ORAL |
Start Marketing Date | 20090801 |
Marketing Category Name | ANDA |
Labeler Name | KAISER FOUNDATION HOSPITALS |
Substance Name | OMEPRAZOLE |
Strength Number | 40 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |