Amcinonide is a Topical Cream in the Human Prescription Drug category. It is labeled and distributed by Fougera Pharmaceuticals Inc.. The primary component is Amcinonide.
| Product ID | 0168-0278_1a90b281-f4ff-4798-b217-a531a280a77b |
| NDC | 0168-0278 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Amcinonide |
| Generic Name | Amcinonide |
| Dosage Form | Cream |
| Route of Administration | TOPICAL |
| Marketing Start Date | 2003-05-15 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA076065 |
| Labeler Name | Fougera Pharmaceuticals Inc. |
| Substance Name | AMCINONIDE |
| Active Ingredient Strength | 1 mg/g |
| Pharm Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2003-05-15 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA076065 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2003-05-15 |
| Marketing Category | ANDA |
| Application Number | ANDA076065 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2003-05-15 |
| Marketing Category | ANDA |
| Application Number | ANDA076065 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | GM |
| Marketing Start Date | 2003-05-15 |
| Ingredient | Strength |
|---|---|
| AMCINONIDE | 1 mg/g |
| SPL SET ID: | 8aefa477-ac2c-41c8-a807-d24522aed8f0 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0168-0278 | Amcinonide | Amcinonide |
| 0168-0279 | Amcinonide | amcinonide |
| 0168-0280 | amcinonide | amcinonide |
| 51672-4054 | Amcinonide | Amcinonide |
| 51672-4060 | Amcinonide | Amcinonide |