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AVAPTA
AVAPTA - 76332-001-02 - (Menthol)
Drug Information of AVAPTA
| Product NDC: | 76332-001 |
| Proprietary Name: | AVAPTA |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 4 g/100g & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AVAPTA
| Product NDC: | 76332-001 |
| Labeler Name: | Neel Products LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110901 |
Package Information of AVAPTA
| Package NDC: | 76332-001-02 |
| Package Description: | 226 g in 1 BOTTLE (76332-001-02) |
NDC Information of AVAPTA
| NDC Code | 76332-001-02 |
| Proprietary Name | AVAPTA |
| Package Description | 226 g in 1 BOTTLE (76332-001-02) |
| Product NDC | 76332-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Neel Products LLC |
| Substance Name | MENTHOL |
| Strength Number | 4 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
