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Fluoxetine
Fluoxetine - 51079-971-19 - (fluoxetine hydrochloride)
Drug Information of Fluoxetine
| Product NDC: | 51079-971 |
| Proprietary Name: | Fluoxetine |
| Non Proprietary Name: | fluoxetine hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; fluoxetine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluoxetine
| Product NDC: | 51079-971 |
| Labeler Name: | UDL Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075207 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110711 |
Package Information of Fluoxetine
| Package NDC: | 51079-971-19 |
| Package Description: | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-971-19) > 1 CAPSULE in 1 BLISTER PACK (51079-971-17) |
NDC Information of Fluoxetine
| NDC Code | 51079-971-19 |
| Proprietary Name | Fluoxetine |
| Package Description | 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-971-19) > 1 CAPSULE in 1 BLISTER PACK (51079-971-17) |
| Product NDC | 51079-971 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluoxetine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20110711 |
| Marketing Category Name | ANDA |
| Labeler Name | UDL Laboratories, Inc. |
| Substance Name | FLUOXETINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
