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Maprotiline Hydrochloride
Maprotiline Hydrochloride - 0378-0060-01 - (maprotiline hydrochloride)
Drug Information of Maprotiline Hydrochloride
| Product NDC: | 0378-0060 |
| Proprietary Name: | Maprotiline Hydrochloride |
| Non Proprietary Name: | maprotiline hydrochloride |
| Active Ingredient(s): | 25 mg/1 & nbsp; maprotiline hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Maprotiline Hydrochloride
| Product NDC: | 0378-0060 |
| Labeler Name: | Mylan Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072285 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121105 |
Package Information of Maprotiline Hydrochloride
| Package NDC: | 0378-0060-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0060-01) |
NDC Information of Maprotiline Hydrochloride
| NDC Code | 0378-0060-01 |
| Proprietary Name | Maprotiline Hydrochloride |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0060-01) |
| Product NDC | 0378-0060 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | maprotiline hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20121105 |
| Marketing Category Name | ANDA |
| Labeler Name | Mylan Pharmaceuticals Inc. |
| Substance Name | MAPROTILINE HYDROCHLORIDE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
