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: | 0527-1729-74 |
Package Description: | 4 mL in 1 BOTTLE, GLASS (0527-1729-74) |
NDC Code | 0527-1729-74 |
Proprietary Name | Cocaine Hydrochloride |
Package Description | 4 mL in 1 BOTTLE, GLASS (0527-1729-74) |
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 |