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ANAFRANIL
ANAFRANIL - 0406-9907-03 - (clomipramine hydrochloride)
Drug Information of ANAFRANIL
| Product NDC: | 0406-9907 |
| Proprietary Name: | ANAFRANIL |
| Non Proprietary Name: | clomipramine hydrochloride |
| Active Ingredient(s): | 50 mg/1 & nbsp; clomipramine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ANAFRANIL
| Product NDC: | 0406-9907 |
| Labeler Name: | Mallinckrodt, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019906 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110318 |
Package Information of ANAFRANIL
| Package NDC: | 0406-9907-03 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (0406-9907-03) |
NDC Information of ANAFRANIL
| NDC Code | 0406-9907-03 |
| Proprietary Name | ANAFRANIL |
| Package Description | 30 CAPSULE in 1 BOTTLE (0406-9907-03) |
| Product NDC | 0406-9907 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | clomipramine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110318 |
| Marketing Category Name | NDA |
| Labeler Name | Mallinckrodt, Inc. |
| Substance Name | CLOMIPRAMINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
