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PRILOSEC
PRILOSEC - 0186-0743-82 - (Omeprazole magnesium)
Drug Information of PRILOSEC
| Product NDC: | 0186-0743 |
| Proprietary Name: | PRILOSEC |
| Non Proprietary Name: | Omeprazole magnesium |
| Active Ingredient(s): | 40 mg/1 & nbsp; Omeprazole magnesium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRILOSEC
| Product NDC: | 0186-0743 |
| Labeler Name: | AstraZeneca LP |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019810 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19980608 |
Package Information of PRILOSEC
| Package NDC: | 0186-0743-82 |
| Package Description: | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0186-0743-82) |
NDC Information of PRILOSEC
| NDC Code | 0186-0743-82 |
| Proprietary Name | PRILOSEC |
| Package Description | 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0186-0743-82) |
| Product NDC | 0186-0743 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Omeprazole magnesium |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 19980608 |
| Marketing Category Name | NDA |
| Labeler Name | AstraZeneca LP |
| Substance Name | OMEPRAZOLE MAGNESIUM |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
