Product NDC: | 0472-0730 |
Proprietary Name: | Miconazole 7 |
Non Proprietary Name: | Miconazole Nitrate |
Active Ingredient(s): | 2 g/100g & nbsp; Miconazole Nitrate |
Administration Route(s): | VAGINAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0472-0730 |
Labeler Name: | Actavis Mid Atlantic LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA074164 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110916 |
Package NDC: | 0472-0730-63 |
Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (0472-0730-63) > 45 g in 1 TUBE, WITH APPLICATOR |
NDC Code | 0472-0730-63 |
Proprietary Name | Miconazole 7 |
Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (0472-0730-63) > 45 g in 1 TUBE, WITH APPLICATOR |
Product NDC | 0472-0730 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Miconazole Nitrate |
Dosage Form Name | CREAM |
Route Name | VAGINAL |
Start Marketing Date | 20110916 |
Marketing Category Name | ANDA |
Labeler Name | Actavis Mid Atlantic LLC |
Substance Name | MICONAZOLE NITRATE |
Strength Number | 2 |
Strength Unit | g/100g |
Pharmaceutical Classes |