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miconazole 1
miconazole 1 - 37808-737-45 - (Miconazole nitrate)
Drug Information of miconazole 1
| Product NDC: | 37808-737 |
| Proprietary Name: | miconazole 1 |
| Non Proprietary Name: | Miconazole nitrate |
| Active Ingredient(s): | & nbsp; Miconazole nitrate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of miconazole 1
| Product NDC: | 37808-737 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079114 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100607 |
Package Information of miconazole 1
| Package NDC: | 37808-737-45 |
| Package Description: | 1 KIT in 1 CARTON (37808-737-45) * 1 BLISTER PACK in 1 KIT > 1 INSERT in 1 BLISTER PACK * 1 TUBE in 1 KIT > 9 g in 1 TUBE * 3 PACKAGE in 1 KIT > 1 SWAB in 1 PACKAGE |
NDC Information of miconazole 1
| NDC Code | 37808-737-45 |
| Proprietary Name | miconazole 1 |
| Package Description | 1 KIT in 1 CARTON (37808-737-45) * 1 BLISTER PACK in 1 KIT > 1 INSERT in 1 BLISTER PACK * 1 TUBE in 1 KIT > 9 g in 1 TUBE * 3 PACKAGE in 1 KIT > 1 SWAB in 1 PACKAGE |
| Product NDC | 37808-737 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole nitrate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20100607 |
| Marketing Category Name | ANDA |
| Labeler Name | H E B |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
