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Fluphenazine Hydrochloride
Fluphenazine Hydrochloride - 51079-487-20 - (fluphenazine hydrochloride)
Drug Information of Fluphenazine Hydrochloride
| Product NDC: | 51079-487 |
| Proprietary Name: | Fluphenazine Hydrochloride |
| Non Proprietary Name: | fluphenazine hydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; fluphenazine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluphenazine Hydrochloride
| Product NDC: | 51079-487 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089804 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110715 |
Package Information of Fluphenazine Hydrochloride
| Package NDC: | 51079-487-20 |
| Package Description: | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-487-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-487-01) |
NDC Information of Fluphenazine Hydrochloride
| NDC Code | 51079-487-20 |
| Proprietary Name | Fluphenazine Hydrochloride |
| Package Description | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-487-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-487-01) |
| Product NDC | 51079-487 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluphenazine hydrochloride |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110715 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | FLUPHENAZINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |
