Home
>
National Drug Code (NDC)
>
Prilosec OTC
Prilosec OTC - 37000-459-05 - (OMEPRAZOLE MAGNESIUM)
Drug Information of Prilosec OTC
| Product NDC: | 37000-459 |
| Proprietary Name: | Prilosec OTC |
| Non Proprietary Name: | OMEPRAZOLE MAGNESIUM |
| Active Ingredient(s): | 20.6 mg/1 & nbsp; OMEPRAZOLE MAGNESIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prilosec OTC
| Product NDC: | 37000-459 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021229 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120815 |
Package Information of Prilosec OTC
| Package NDC: | 37000-459-05 |
| Package Description: | 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK (37000-459-05) |
NDC Information of Prilosec OTC
| NDC Code | 37000-459-05 |
| Proprietary Name | Prilosec OTC |
| Package Description | 14 TABLET, DELAYED RELEASE in 1 BLISTER PACK (37000-459-05) |
| Product NDC | 37000-459 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OMEPRAZOLE MAGNESIUM |
| Dosage Form Name | TABLET, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120815 |
| Marketing Category Name | NDA |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | OMEPRAZOLE MAGNESIUM |
| Strength Number | 20.6 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
