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PROPAFENONE HYDROCHLORIDE
PROPAFENONE HYDROCHLORIDE - 51079-996-20 - (propafenone hydrochloride)
Drug Information of PROPAFENONE HYDROCHLORIDE
| Product NDC: | 51079-996 |
| Proprietary Name: | PROPAFENONE HYDROCHLORIDE |
| Non Proprietary Name: | propafenone hydrochloride |
| Active Ingredient(s): | 150 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 HYDROCHLORIDE
| Product NDC: | 51079-996 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075998 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110520 |
Package Information of PROPAFENONE HYDROCHLORIDE
| Package NDC: | 51079-996-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-996-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-996-01) |
NDC Information of PROPAFENONE HYDROCHLORIDE
| NDC Code | 51079-996-20 |
| Proprietary Name | PROPAFENONE HYDROCHLORIDE |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-996-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-996-01) |
| Product NDC | 51079-996 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | propafenone hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110520 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | PROPAFENONE HYDROCHLORIDE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antiarrhythmic [EPC] |
