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Anti-Diarrheal
Anti-Diarrheal - 49348-752-04 - (LOPERAMIDE HYDROCHLORIDE)
Drug Information of Anti-Diarrheal
| Product NDC: | 49348-752 |
| Proprietary Name: | Anti-Diarrheal |
| Non Proprietary Name: | LOPERAMIDE HYDROCHLORIDE |
| Active Ingredient(s): | 2 mg/1 & nbsp; LOPERAMIDE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Anti-Diarrheal
| Product NDC: | 49348-752 |
| Labeler Name: | Mckesson (Sunmark) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021855 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100709 |
Package Information of Anti-Diarrheal
| Package NDC: | 49348-752-04 |
| Package Description: | 2 BLISTER PACK in 1 BOX (49348-752-04) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of Anti-Diarrheal
| NDC Code | 49348-752-04 |
| Proprietary Name | Anti-Diarrheal |
| Package Description | 2 BLISTER PACK in 1 BOX (49348-752-04) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 49348-752 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | LOPERAMIDE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20100709 |
| Marketing Category Name | NDA |
| Labeler Name | Mckesson (Sunmark) |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
