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lansoprazole
lansoprazole - 37808-117-03 - (Lansoprazole)
Drug Information of lansoprazole
| Product NDC: | 37808-117 |
| Proprietary Name: | lansoprazole |
| Non Proprietary Name: | Lansoprazole |
| Active Ingredient(s): | 15 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: | 37808-117 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA202319 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120518 |
Package Information of lansoprazole
| Package NDC: | 37808-117-03 |
| Package Description: | 3 BOTTLE in 1 CARTON (37808-117-03) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
NDC Information of lansoprazole
| NDC Code | 37808-117-03 |
| Proprietary Name | lansoprazole |
| Package Description | 3 BOTTLE in 1 CARTON (37808-117-03) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE |
| Product NDC | 37808-117 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Lansoprazole |
| Dosage Form Name | CAPSULE, DELAYED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120518 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | LANSOPRAZOLE |
| Strength Number | 15 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
