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PRUDOXIN
PRUDOXIN - 0064-3600-45 - (doxepin hydrochloride)
Drug Information of PRUDOXIN
| Product NDC: | 0064-3600 |
| Proprietary Name: | PRUDOXIN |
| Non Proprietary Name: | doxepin hydrochloride |
| Active Ingredient(s): | 50 mg/g & nbsp; doxepin hydrochloride |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of PRUDOXIN
| Product NDC: | 0064-3600 |
| Labeler Name: | HEALTHPOINT, LTD |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020126 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20011001 |
Package Information of PRUDOXIN
| Package NDC: | 0064-3600-45 |
| Package Description: | 45 g in 1 TUBE (0064-3600-45) |
NDC Information of PRUDOXIN
| NDC Code | 0064-3600-45 |
| Proprietary Name | PRUDOXIN |
| Package Description | 45 g in 1 TUBE (0064-3600-45) |
| Product NDC | 0064-3600 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | doxepin hydrochloride |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20011001 |
| Marketing Category Name | NDA |
| Labeler Name | HEALTHPOINT, LTD |
| Substance Name | DOXEPIN HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
