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Omeprazole Magnesium
Omeprazole Magnesium - 55111-397-42 - (Omeprazole Magnesium)
Drug Information of Omeprazole Magnesium
| Product NDC: | 55111-397 |
| Proprietary Name: | Omeprazole Magnesium |
| Non Proprietary Name: | Omeprazole Magnesium |
| Active Ingredient(s): | 20 mg/1 & nbsp; Omeprazole Magnesium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Omeprazole Magnesium
| Product NDC: | 55111-397 |
| Labeler Name: | Dr. Reddy's Laboratories Limited |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA078878 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091112 |
Package Information of Omeprazole Magnesium
| Package NDC: | 55111-397-42 |
| Package Description: | 3 CARTON in 1 CARTON (55111-397-42) > 2 BLISTER PACK in 1 CARTON (55111-397-74) > 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
NDC Information of Omeprazole Magnesium
| NDC Code | 55111-397-42 |
| Proprietary Name | Omeprazole Magnesium |
| Package Description | 3 CARTON in 1 CARTON (55111-397-42) > 2 BLISTER PACK in 1 CARTON (55111-397-74) > 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
| Product NDC | 55111-397 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Omeprazole Magnesium |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20091112 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr. Reddy's Laboratories Limited |
| Substance Name | OMEPRAZOLE MAGNESIUM |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
