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Etodolac
Etodolac - 0185-0139-05 - (Etodolac)
Drug Information of Etodolac
| Product NDC: | 0185-0139 |
| Proprietary Name: | Etodolac |
| Non Proprietary Name: | Etodolac |
| Active Ingredient(s): | 500 mg/1 & nbsp; Etodolac |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Etodolac
| Product NDC: | 0185-0139 |
| Labeler Name: | Eon Labs, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074903 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19990419 |
Package Information of Etodolac
| Package NDC: | 0185-0139-05 |
| Package Description: | 500 TABLET, COATED in 1 BOTTLE (0185-0139-05) |
NDC Information of Etodolac
| NDC Code | 0185-0139-05 |
| Proprietary Name | Etodolac |
| Package Description | 500 TABLET, COATED in 1 BOTTLE (0185-0139-05) |
| Product NDC | 0185-0139 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Etodolac |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 19990419 |
| Marketing Category Name | ANDA |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | ETODOLAC |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
