Cymbalta is a Oral Capsule, Delayed Release in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Duloxetine Hydrochloride.
Product ID | 70518-2099_8996ad9d-6d26-7ef3-e053-2995a90ab61f |
NDC | 70518-2099 |
Product Type | Human Prescription Drug |
Proprietary Name | Cymbalta |
Generic Name | Duloxetine Hydrochloride |
Dosage Form | Capsule, Delayed Release |
Route of Administration | ORAL |
Marketing Start Date | 2019-05-22 |
Marketing Category | NDA / NDA |
Application Number | NDA021427 |
Labeler Name | REMEDYREPACK INC. |
Substance Name | DULOXETINE HYDROCHLORIDE |
Active Ingredient Strength | 30 mg/1 |
Pharm Classes | Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2019-05-22 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA021427 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2019-05-22 |
Ingredient | Strength |
---|---|
DULOXETINE HYDROCHLORIDE | 30 mg/1 |
SPL SET ID: | 1beb5954-fdb2-47d0-9ca1-586df00ba915 |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
0002-3235 | Cymbalta | Duloxetine hydrochloride |
0002-3240 | Cymbalta | Duloxetine hydrochloride |
0002-3270 | Cymbalta | Duloxetine hydrochloride |
21695-145 | Cymbalta | Duloxetine hydrochloride |
21695-146 | Cymbalta | Duloxetine hydrochloride |
68151-4734 | Cymbalta | Cymbalta |
68151-4679 | Cymbalta | Cymbalta |
21695-657 | Cymbalta | Cymbalta |
35356-843 | Cymbalta | Cymbalta |
43353-303 | Cymbalta | Cymbalta |
49999-618 | Cymbalta | Cymbalta |
52959-892 | Cymbalta | Cymbalta |
55289-028 | Cymbalta | Cymbalta |
55289-036 | Cymbalta | Cymbalta |
70518-2100 | Cymbalta | Cymbalta |
70518-2099 | Cymbalta | Cymbalta |
80425-0086 | Cymbalta | Cymbalta |
80425-0119 | Cymbalta | Cymbalta |
0904-7043 | Duloxetine | Duloxetine Hydrochloride |
0904-7044 | Duloxetine | Duloxetine Hydrochloride |
0904-7045 | Duloxetine | Duloxetine Hydrochloride |
0615-8034 | Duloxetine Hydrochloride | Duloxetine Hydrochloride |
0615-8035 | Duloxetine Hydrochloride | Duloxetine Hydrochloride |
0904-6452 | Duloxetine Hydrochloride | Duloxetine Hydrochloride |
0904-6453 | Duloxetine Hydrochloride | Duloxetine Hydrochloride |
0904-6454 | Duloxetine Hydrochloride | Duloxetine Hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CYMBALTA 78859969 3194152 Live/Registered |
Eli Lilly and Company 2006-04-12 |
CYMBALTA 76535580 not registered Dead/Abandoned |
Eli Lilly and Company 2003-07-25 |
CYMBALTA 75867543 2802665 Live/Registered |
Eli Lilly and Company 1999-12-09 |