| Product NDC: | 0527-1729 |
| Proprietary Name: | Cocaine Hydrochloride |
| Non Proprietary Name: | Cocaine Hydrochloride |
| Active Ingredient(s): | 100 mg/mL & nbsp; Cocaine Hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0527-1729 |
| Labeler Name: | Lannett Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20081201 |
| Package NDC: | 0527-1729-73 |
| Package Description: | 10 mL in 1 BOTTLE (0527-1729-73) |
| NDC Code | 0527-1729-73 |
| Proprietary Name | Cocaine Hydrochloride |
| Package Description | 10 mL in 1 BOTTLE (0527-1729-73) |
| Product NDC | 0527-1729 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cocaine Hydrochloride |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20081201 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Lannett Company, Inc. |
| Substance Name | COCAINE HYDROCHLORIDE |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |