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Doxepin Hydrochloride
Doxepin Hydrochloride - 50436-4565-1 - (doxepin hydrochloride)
Drug Information of Doxepin Hydrochloride
| Product NDC: | 50436-4565 |
| Proprietary Name: | Doxepin Hydrochloride |
| Non Proprietary Name: | doxepin hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; doxepin hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Doxepin Hydrochloride
| Product NDC: | 50436-4565 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070791 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110504 |
Package Information of Doxepin Hydrochloride
| Package NDC: | 50436-4565-1 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (50436-4565-1) |
NDC Information of Doxepin Hydrochloride
| NDC Code | 50436-4565-1 |
| Proprietary Name | Doxepin Hydrochloride |
| Package Description | 30 CAPSULE in 1 BOTTLE (50436-4565-1) |
| Product NDC | 50436-4565 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | doxepin hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110504 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | DOXEPIN HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
