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DOXEPIN HYDROCHLORIDE
DOXEPIN HYDROCHLORIDE - 24236-933-24 - (DOXEPIN HYDROCHLORIDE)
Drug Information of DOXEPIN HYDROCHLORIDE
| Product NDC: | 24236-933 |
| 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: | 24236-933 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA070791 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101217 |
Package Information of DOXEPIN HYDROCHLORIDE
| Package NDC: | 24236-933-24 |
| Package Description: | 200 CAPSULE in 1 CANISTER (24236-933-24) |
NDC Information of DOXEPIN HYDROCHLORIDE
| NDC Code | 24236-933-24 |
| Proprietary Name | DOXEPIN HYDROCHLORIDE |
| Package Description | 200 CAPSULE in 1 CANISTER (24236-933-24) |
| Product NDC | 24236-933 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | DOXEPIN HYDROCHLORIDE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20101217 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | DOXEPIN HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
