Etodolac is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Lake Erie Medical Dba Quality Care Products Llc. The primary component is Etodolac.
Product ID | 35356-826_1d4d5ad3-394b-4574-b4d3-f35eec6bebb5 |
NDC | 35356-826 |
Product Type | Human Prescription Drug |
Proprietary Name | Etodolac |
Generic Name | Etodolac |
Dosage Form | Tablet, Film Coated |
Route of Administration | ORAL |
Marketing Start Date | 1998-05-20 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA075009 |
Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | ETODOLAC |
Active Ingredient Strength | 400 mg/1 |
Pharm Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 1998-05-20 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA075009 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-05-20 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA075009 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-05-20 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA075009 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 1998-05-20 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA075009 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-05-20 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA075009 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-05-20 |
Marketing End Date | 2018-12-31 |
Marketing Category | ANDA |
Application Number | ANDA075009 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 1998-05-20 |
Marketing End Date | 2018-12-31 |
Ingredient | Strength |
---|---|
ETODOLAC | 400 mg/1 |
SPL SET ID: | 1714328a-3e1a-45e0-83a8-1813c5c7f1f8 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
PHarm Class EPC | |
NUI Code |
NDC | Brand Name | Generic Name |
---|---|---|
0093-0892 | Etodolac | Etodolac |
0093-1118 | Etodolac | Etodolac |
0093-1122 | Etodolac | Etodolac |
0093-1893 | Etodolac | Etodolac |
0093-7172 | Etodolac | Etodolac |
0185-0675 | Etodolac | Etodolac |
0185-0687 | Etodolac | Etodolac |
10544-862 | Etodolac | Etodolac |
16714-497 | Etodolac | Etodolac |
16714-498 | Etodolac | Etodolac |
16714-499 | Etodolac | Etodolac |
21695-049 | Etodolac | Etodolac |
21695-050 | Etodolac | Etodolac |
33261-043 | Etodolac | Etodolac |
33261-044 | Etodolac | Etodolac |
35356-324 | Etodolac | Etodolac |
35356-711 | Etodolac | Etodolac |
35356-826 | Etodolac | Etodolac |
42254-052 | Etodolac | Etodolac |
42254-121 | Etodolac | etodolac |
42291-404 | Etodolac | Etodolac |
42291-405 | Etodolac | Etodolac |
42799-111 | Etodolac | Etodolac |
68151-0738 | Etodolac | Etodolac |
68382-273 | Etodolac | Etodolac |
68382-271 | Etodolac | Etodolac |
68382-272 | Etodolac | Etodolac |
68788-6901 | Etodolac | Etodolac |
68788-9410 | Etodolac | Etodolac |
68788-7315 | Etodolac | Etodolac |
68788-7300 | Etodolac | Etodolac |
68788-7068 | Etodolac | Etodolac |
68788-9928 | Etodolac | Etodolac |
68788-9929 | Etodolac | Etodolac |
68788-9360 | Etodolac | Etodolac |
68788-9990 | Etodolac | Etodolac |
68788-9930 | Etodolac | Etodolac |
69238-1342 | Etodolac | Etodolac |
69238-1343 | Etodolac | Etodolac |
70332-320 | Etodolac | Etodolac |
71335-0092 | Etodolac | Etodolac |
71335-0183 | Etodolac | Etodolac |
71335-0399 | Etodolac | Etodolac |
71335-0602 | Etodolac | Etodolac |
71335-0640 | Etodolac | Etodolac |
71335-0126 | Etodolac | Etodolac |
71335-0982 | Etodolac | Etodolac |
43063-578 | Etodolac | Etodolac |
42799-112 | Etodolac | Etodolac |
43063-671 | Etodolac | Etodolac |