61919-858 : Etodolac 500 mg Oral Tablet, Film Coated
NDC: | 61919-858 |
Labeler: | Direct Rx |
Product Type: | Human Prescription Drug |
Drug Name: | Etodolac |
Dosage Form: | Oral Tablet, Film Coated |
Application #: | ANDA076004 |
Rev. Date: |
Appearance:
Markings: | APO;102;500 |
Shapes: |
Oval |
Colors: |
White |
Size (mm): | 19 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 61919-858-30: 30 TABLET, FILM COATED IN 1 BOTTLE (61919‑858‑30)
Active Ingredients:
- Etodolac
Dosage Strength:
- 500 mg
Inactive Ingredients:
- Magnesium Stearate
- Titanium Dioxide
- Crospovidone (15 Mpa.s At 5%)
- Hypromellose 2208 (100 Mpa.s)
- Methylcellulose (100 Cps)
- Polyethylene Glycol 1500 /
Pharmaceutical Classes:
- Anti-Inflammatory Agents
- Non-Steroidal [CS]
- Cyclooxygenase Inhibitors [MoA]
- Nonsteroidal Anti-inflammatory Drug [EPC]
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- 0179-0207 Etodolac 400 mg Oral Tablet, Film Coated by Kaiser Foundation Hospitals
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- 16590-092 Etodolac 400 mg Oral Tablet by Stat Rx USA LLC
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NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.