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PRILOSEC
PRILOSEC - 16590-334-30 - (OMEPRAZOLE MAGNESIUM)
Drug Information of PRILOSEC
| Product NDC: | 16590-334 |
| Proprietary Name: | PRILOSEC |
| Non Proprietary Name: | OMEPRAZOLE MAGNESIUM |
| Active Ingredient(s): | 20 mg/1 & nbsp; OMEPRAZOLE MAGNESIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRILOSEC
| Product NDC: | 16590-334 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019810 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090930 |
Package Information of PRILOSEC
| Package NDC: | 16590-334-30 |
| Package Description: | 30 CAPSULE in 1 BOTTLE, PLASTIC (16590-334-30) |
NDC Information of PRILOSEC
| NDC Code | 16590-334-30 |
| Proprietary Name | PRILOSEC |
| Package Description | 30 CAPSULE in 1 BOTTLE, PLASTIC (16590-334-30) |
| Product NDC | 16590-334 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | OMEPRAZOLE MAGNESIUM |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20090930 |
| Marketing Category Name | NDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | OMEPRAZOLE MAGNESIUM |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
