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Anti-Diarrheal
Anti-Diarrheal - 50844-375-22 - (Loperamide HCl)
Drug Information of Anti-Diarrheal
| Product NDC: | 50844-375 |
| Proprietary Name: | Anti-Diarrheal |
| Non Proprietary Name: | Loperamide HCl |
| Active Ingredient(s): | 2 mg/1 & nbsp; Loperamide HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anti-Diarrheal
| Product NDC: | 50844-375 |
| Labeler Name: | L.N.K. International, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076497 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050503 |
Package Information of Anti-Diarrheal
| Package NDC: | 50844-375-22 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (50844-375-22) > 48 TABLET in 1 BOTTLE, PLASTIC |
NDC Information of Anti-Diarrheal
| NDC Code | 50844-375-22 |
| Proprietary Name | Anti-Diarrheal |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (50844-375-22) > 48 TABLET in 1 BOTTLE, PLASTIC |
| Product NDC | 50844-375 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loperamide HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050503 |
| Marketing Category Name | ANDA |
| Labeler Name | L.N.K. International, Inc. |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
