Cocaine Hydrochloride is a Topical Solution in the Human Prescription Drug category. It is labeled and distributed by Lannett Company, Inc.. The primary component is Cocaine Hydrochloride.
| Product ID | 0527-1729_094f1141-b41b-4ca0-bc04-6e9cca5df1c9 |
| NDC | 0527-1729 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Cocaine Hydrochloride |
| Generic Name | Cocaine Hydrochloride |
| Dosage Form | Solution |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2008-12-01 |
| Marketing End Date | 2020-08-31 |
| Marketing Category | UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER |
| Labeler Name | Lannett Company, Inc. |
| Substance Name | COCAINE HYDROCHLORIDE |
| Active Ingredient Strength | 100 mg/mL |
| DEA Schedule | CII |
| NDC Exclude Flag | N |
| Marketing Start Date | 2008-12-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2008-12-01 |
| Marketing End Date | 2020-08-31 |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2008-12-01 |
| Marketing End Date | 2020-08-31 |
| Ingredient | Strength |
|---|---|
| COCAINE HYDROCHLORIDE | 100 mg/mL |
| SPL SET ID: | 24faa247-fe12-4574-881d-445b078b3e87 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0527-1728 | Cocaine Hydrochloride | Cocaine Hydrochloride |
| 0527-1729 | Cocaine Hydrochloride | Cocaine Hydrochloride |
| 64950-362 | cocaine hydrochloride | cocaine hydrochloride |
| 64950-359 | GOPRELTO | cocaine hydrochloride |