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Omeprazole
Omeprazole - 21695-617-90 - (Omeprazole)
Drug Information of Omeprazole
| Product NDC: | 21695-617 |
| Proprietary Name: | Omeprazole |
| Non Proprietary Name: | Omeprazole |
| Active Ingredient(s): | 40 mg/1 & nbsp; Omeprazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Omeprazole
| Product NDC: | 21695-617 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075576 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101013 |
Package Information of Omeprazole
| Package NDC: | 21695-617-90 |
| Package Description: | 90 CAPSULE in 1 BOTTLE (21695-617-90) |
NDC Information of Omeprazole
| NDC Code | 21695-617-90 |
| Proprietary Name | Omeprazole |
| Package Description | 90 CAPSULE in 1 BOTTLE (21695-617-90) |
| Product NDC | 21695-617 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Omeprazole |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20101013 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | OMEPRAZOLE |
| Strength Number | 40 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
