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Entacapone
Entacapone - 55648-711-04 - (Entacapone)
Drug Information of Entacapone
| Product NDC: | 55648-711 |
| Proprietary Name: | Entacapone |
| Non Proprietary Name: | Entacapone |
| Active Ingredient(s): | 200 mg/1 & nbsp; Entacapone |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Entacapone
| Product NDC: | 55648-711 |
| Labeler Name: | Wockhardt Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078941 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120816 |
Package Information of Entacapone
| Package NDC: | 55648-711-04 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (55648-711-04) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Entacapone
| NDC Code | 55648-711-04 |
| Proprietary Name | Entacapone |
| Package Description | 10 BLISTER PACK in 1 CARTON (55648-711-04) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 55648-711 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Entacapone |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120816 |
| Marketing Category Name | ANDA |
| Labeler Name | Wockhardt Limited |
| Substance Name | ENTACAPONE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Catechol O-Methyltransferase Inhibitors [MoA],Catechol-O-Methyltransferase Inhibitor [EPC] |
