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Lansoprazole
Lansoprazole - 54868-6205-0 - (Lansoprazole)
Drug Information of Lansoprazole
| Product NDC: | 54868-6205 |
| Proprietary Name: | Lansoprazole |
| Non Proprietary Name: | Lansoprazole |
| Active Ingredient(s): | 30 mg/1 & nbsp; Lansoprazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lansoprazole
| Product NDC: | 54868-6205 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078730 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101130 |
Package Information of Lansoprazole
| Package NDC: | 54868-6205-0 |
| Package Description: | 3 BLISTER PACK in 1 BOTTLE, PLASTIC (54868-6205-0) > 10 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK |
NDC Information of Lansoprazole
| NDC Code | 54868-6205-0 |
| Proprietary Name | Lansoprazole |
| Package Description | 3 BLISTER PACK in 1 BOTTLE, PLASTIC (54868-6205-0) > 10 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK |
| Product NDC | 54868-6205 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lansoprazole |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20101130 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | LANSOPRAZOLE |
| Strength Number | 30 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA] |
