Home
>
National Drug Code (NDC)
>
OMEPRAZOLE
OMEPRAZOLE - 42549-658-60 - (OMEPRAZOLE)
Drug Information of OMEPRAZOLE
| Product NDC: | 42549-658 |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of OMEPRAZOLE
| Product NDC: | 42549-658 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078490 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090417 |
Package Information of OMEPRAZOLE
| Package NDC: | 42549-658-60 |
| Package Description: | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42549-658-60) |
NDC Information of OMEPRAZOLE
| NDC Code | 42549-658-60 |
| Proprietary Name | OMEPRAZOLE |
| Package Description | 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42549-658-60) |
| Product NDC | 42549-658 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | OMEPRAZOLE |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090417 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | OMEPRAZOLE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
