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Equaline
Equaline - 41163-812-72 - (Menthol)
Drug Information of Equaline
| Product NDC: | 41163-812 |
| Proprietary Name: | Equaline |
| Non Proprietary Name: | Menthol |
| Active Ingredient(s): | 50 mg/1 & nbsp; Menthol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | PATCH |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Equaline
| Product NDC: | 41163-812 |
| Labeler Name: | Supervalu Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part348 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100705 |
Package Information of Equaline
| Package NDC: | 41163-812-72 |
| Package Description: | 1 POUCH in 1 CARTON (41163-812-72) > 5 PATCH in 1 POUCH |
NDC Information of Equaline
| NDC Code | 41163-812-72 |
| Proprietary Name | Equaline |
| Package Description | 1 POUCH in 1 CARTON (41163-812-72) > 5 PATCH in 1 POUCH |
| Product NDC | 41163-812 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Menthol |
| Dosage Form Name | PATCH |
| Route Name | TOPICAL |
| Start Marketing Date | 20100705 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Supervalu Inc. |
| Substance Name | MENTHOL |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
