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Prochlorperazine
Prochlorperazine - 0713-0135-10 - (Prochlorperazine)
Drug Information of Prochlorperazine
| Product NDC: | 0713-0135 |
| Proprietary Name: | Prochlorperazine |
| Non Proprietary Name: | Prochlorperazine |
| Active Ingredient(s): | 25 mg/1 & nbsp; Prochlorperazine |
| Administration Route(s): | RECTAL |
| Dosage Form(s): | SUPPOSITORY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Prochlorperazine
| Product NDC: | 0713-0135 |
| Labeler Name: | G & W LABORATORIES, INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040058 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19931130 |
Package Information of Prochlorperazine
| Package NDC: | 0713-0135-10 |
| Package Description: | 1000 SUPPOSITORY in 1 PACKAGE (0713-0135-10) |
NDC Information of Prochlorperazine
| NDC Code | 0713-0135-10 |
| Proprietary Name | Prochlorperazine |
| Package Description | 1000 SUPPOSITORY in 1 PACKAGE (0713-0135-10) |
| Product NDC | 0713-0135 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Prochlorperazine |
| Dosage Form Name | SUPPOSITORY |
| Route Name | RECTAL |
| Start Marketing Date | 19931130 |
| Marketing Category Name | ANDA |
| Labeler Name | G & W LABORATORIES, INC. |
| Substance Name | PROCHLORPERAZINE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
