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Keratol 45
Keratol 45 - 51991-701-41 - (Urea)
Drug Information of Keratol 45
| Product NDC: | 51991-701 |
| Proprietary Name: | Keratol 45 |
| Non Proprietary Name: | Urea |
| Active Ingredient(s): | 450 mg/g & nbsp; Urea |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Keratol 45
| Product NDC: | 51991-701 |
| Labeler Name: | Breckenridge Pharmaceutical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20100125 |
Package Information of Keratol 45
| Package NDC: | 51991-701-41 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (51991-701-41) > 28 g in 1 BOTTLE, GLASS |
NDC Information of Keratol 45
| NDC Code | 51991-701-41 |
| Proprietary Name | Keratol 45 |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (51991-701-41) > 28 g in 1 BOTTLE, GLASS |
| Product NDC | 51991-701 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Urea |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100125 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Breckenridge Pharmaceutical Inc. |
| Substance Name | UREA |
| Strength Number | 450 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
