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Omeprazole Delayed-Release
Omeprazole Delayed-Release - 63304-445-01 - (Omeprazole)
Drug Information of Omeprazole Delayed-Release
| Product NDC: | 63304-445 |
| Proprietary Name: | Omeprazole Delayed-Release |
| Non Proprietary Name: | Omeprazole |
| Active Ingredient(s): | 40 mg/1 & nbsp; Omeprazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Omeprazole Delayed-Release
| Product NDC: | 63304-445 |
| Labeler Name: | Ranbaxy Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019810 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20080725 |
Package Information of Omeprazole Delayed-Release
| Package NDC: | 63304-445-01 |
| Package Description: | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63304-445-01) |
NDC Information of Omeprazole Delayed-Release
| NDC Code | 63304-445-01 |
| Proprietary Name | Omeprazole Delayed-Release |
| Package Description | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63304-445-01) |
| Product NDC | 63304-445 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Omeprazole |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20080725 |
| Marketing Category Name | NDA |
| Labeler Name | Ranbaxy Laboratories Inc. |
| Substance Name | OMEPRAZOLE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
