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TOFRANIL
TOFRANIL - 0406-9921-03 - (imipramine hydrochloride)
Drug Information of TOFRANIL
| Product NDC: | 0406-9921 |
| Proprietary Name: | TOFRANIL |
| Non Proprietary Name: | imipramine hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; imipramine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, SUGAR COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TOFRANIL
| Product NDC: | 0406-9921 |
| Labeler Name: | Mallinckrodt, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087845 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110124 |
Package Information of TOFRANIL
| Package NDC: | 0406-9921-03 |
| Package Description: | 30 TABLET, SUGAR COATED in 1 BOTTLE (0406-9921-03) |
NDC Information of TOFRANIL
| NDC Code | 0406-9921-03 |
| Proprietary Name | TOFRANIL |
| Package Description | 30 TABLET, SUGAR COATED in 1 BOTTLE (0406-9921-03) |
| Product NDC | 0406-9921 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | imipramine hydrochloride |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110124 |
| Marketing Category Name | ANDA |
| Labeler Name | Mallinckrodt, Inc. |
| Substance Name | IMIPRAMINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tricyclic Antidepressant [EPC] |
