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Lansoprazole
Lansoprazole - 55111-399-79 - (lansoprazole)
Drug Information of Lansoprazole
| Product NDC: | 55111-399 |
| Proprietary Name: | Lansoprazole |
| Non Proprietary Name: | lansoprazole |
| Active Ingredient(s): | 30 mg/1 & nbsp; lansoprazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lansoprazole
| Product NDC: | 55111-399 |
| Labeler Name: | Dr.Reddy's Laboratories Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091269 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101015 |
Package Information of Lansoprazole
| Package NDC: | 55111-399-79 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (55111-399-79) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
NDC Information of Lansoprazole
| NDC Code | 55111-399-79 |
| Proprietary Name | Lansoprazole |
| Package Description | 1 BLISTER PACK in 1 CARTON (55111-399-79) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK |
| Product NDC | 55111-399 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lansoprazole |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20101015 |
| Marketing Category Name | ANDA |
| Labeler Name | Dr.Reddy's Laboratories Ltd. |
| Substance Name | LANSOPRAZOLE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
