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ATOPALM TOLNAFTATE ANTIFUNGAL
ATOPALM TOLNAFTATE ANTIFUNGAL - 51141-2000-1 - (TOLNAFTATE)
Drug Information of ATOPALM TOLNAFTATE ANTIFUNGAL
| Product NDC: | 51141-2000 |
| Proprietary Name: | ATOPALM TOLNAFTATE ANTIFUNGAL |
| Non Proprietary Name: | TOLNAFTATE |
| Active Ingredient(s): | 1 g/100g & nbsp; TOLNAFTATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ATOPALM TOLNAFTATE ANTIFUNGAL
| Product NDC: | 51141-2000 |
| Labeler Name: | Neopharm Co., Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110316 |
Package Information of ATOPALM TOLNAFTATE ANTIFUNGAL
| Package NDC: | 51141-2000-1 |
| Package Description: | 1 TUBE in 1 CARTON (51141-2000-1) > 28.3 g in 1 TUBE |
NDC Information of ATOPALM TOLNAFTATE ANTIFUNGAL
| NDC Code | 51141-2000-1 |
| Proprietary Name | ATOPALM TOLNAFTATE ANTIFUNGAL |
| Package Description | 1 TUBE in 1 CARTON (51141-2000-1) > 28.3 g in 1 TUBE |
| Product NDC | 51141-2000 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TOLNAFTATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110316 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Neopharm Co., Ltd. |
| Substance Name | TOLNAFTATE |
| Strength Number | 1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
