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Doxepin Hydrochloride
Doxepin Hydrochloride - 49884-222-01 - (Doxepin Hydrochloride)
Drug Information of Doxepin Hydrochloride
| Product NDC: | 49884-222 |
| Proprietary Name: | Doxepin Hydrochloride |
| Non Proprietary Name: | Doxepin Hydrochloride |
| Active Ingredient(s): | 150 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: | 49884-222 |
| Labeler Name: | Par Pharmaceutical Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA071669 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19871109 |
Package Information of Doxepin Hydrochloride
| Package NDC: | 49884-222-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (49884-222-01) |
NDC Information of Doxepin Hydrochloride
| NDC Code | 49884-222-01 |
| Proprietary Name | Doxepin Hydrochloride |
| Package Description | 100 CAPSULE in 1 BOTTLE (49884-222-01) |
| Product NDC | 49884-222 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Doxepin Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19871109 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical Inc |
| Substance Name | DOXEPIN HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
