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sunmark anti diarrheal
sunmark anti diarrheal - 49348-529-08 - (Loperamide Hydrochloride)
Drug Information of sunmark anti diarrheal
| Product NDC: | 49348-529 |
| Proprietary Name: | sunmark anti diarrheal |
| Non Proprietary Name: | Loperamide Hydrochloride |
| Active Ingredient(s): | 2 mg/1 & nbsp; Loperamide Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunmark anti diarrheal
| Product NDC: | 49348-529 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075232 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030627 |
Package Information of sunmark anti diarrheal
| Package NDC: | 49348-529-08 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-529-08) > 48 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of sunmark anti diarrheal
| NDC Code | 49348-529-08 |
| Proprietary Name | sunmark anti diarrheal |
| Package Description | 1 BOTTLE in 1 CARTON (49348-529-08) > 48 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 49348-529 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Loperamide Hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030627 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | LOPERAMIDE HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
