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Propafenone HCl
Propafenone HCl - 63739-510-10 - (Propafenone hydrochloride)
Drug Information of Propafenone HCl
| Product NDC: | 63739-510 |
| Proprietary Name: | Propafenone HCl |
| Non Proprietary Name: | Propafenone hydrochloride |
| Active Ingredient(s): | 225 mg/1 & nbsp; Propafenone hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Propafenone HCl
| Product NDC: | 63739-510 |
| Labeler Name: | McKesson Packaging Services a business unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075203 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120910 |
Package Information of Propafenone HCl
| Package NDC: | 63739-510-10 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-510-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
NDC Information of Propafenone HCl
| NDC Code | 63739-510-10 |
| Proprietary Name | Propafenone HCl |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-510-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK |
| Product NDC | 63739-510 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Propafenone hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120910 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Packaging Services a business unit of McKesson Corporation |
| Substance Name | PROPAFENONE HYDROCHLORIDE |
| Strength Number | 225 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
