PROCHLORPERAZINE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Pharmpak, Inc.. The primary component is Prochlorperazine Maleate.
| Product ID | 54348-114_8f8754d8-8603-0e64-e053-2995a90a7c21 |
| NDC | 54348-114 |
| Product Type | Human Prescription Drug |
| Proprietary Name | PROCHLORPERAZINE |
| Generic Name | Prochlorperazine |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2019-07-12 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA040268 |
| Labeler Name | PharmPak, Inc. |
| Substance Name | PROCHLORPERAZINE MALEATE |
| Active Ingredient Strength | 10 mg/1 |
| Pharm Classes | Phenothiazine [EPC],Phenothiazines [CS] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2019-07-12 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA040268 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-07-12 |
| Marketing Category | ANDA |
| Application Number | ANDA040268 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2019-07-12 |
| Ingredient | Strength |
|---|---|
| PROCHLORPERAZINE MALEATE | 10 mg/1 |
| SPL SET ID: | 888f253f-1db1-45bc-8fc7-15f97ff0ba18 |
| Manufacturer | |
| UNII |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0713-0135 | Prochlorperazine | Prochlorperazine |
| 50090-0636 | Prochlorperazine | Prochlorperazine |
| 54348-114 | PROCHLORPERAZINE | PROCHLORPERAZINE |
| 54348-989 | Prochlorperazine | PROCHLORPERAZINE |
| 66267-176 | Prochlorperazine | Prochlorperazine |
| 68071-3259 | Prochlorperazine | Prochlorperazine |
| 66213-200 | Compazine | Prochlorperazine |
| 0574-7226 | Compro | PROCHLORPERAZINE |
| 50090-2881 | Compro | PROCHLORPERAZINE |
| 55289-119 | Compro | PROCHLORPERAZINE |
| 63629-8444 | Compro | PROCHLORPERAZINE |