0310-0088 : Daliresp 250 ug/1 Oral Tablet
| NDC: | 0310-0088 |
| Labeler: | Astrazeneca Pharmaceuticals Lp |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Daliresp |
| Dosage Form: | Oral Tablet |
| Application #: | NDA022522 |
| Rev. Date: |
Appearance:
| Markings: | D;250 |
| Shapes: |
Round |
| Colors: |
 White |
| Size (mm): | 5 |
| 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. | |
NDC Package Codes:
- 0310-0088-28: 1 BLISTER PACK IN 1 BOX, UNIT‑DOSE (0310‑0088‑28) > 28 TABLET IN 1 BLISTER PACK
- 0310-0088-39: 10 BLISTER PACK IN 1 BOX, UNIT‑DOSE (0310‑0088‑39) > 2 TABLET IN 1 BLISTER PACK
- 0310-0088-95: 1 BLISTER PACK IN 1 BOX, UNIT‑DOSE (0310‑0088‑95) > 28 TABLET IN 1 BLISTER PACK
Active Ingredients:
- Roflumilast
Dosage Strength:
- 250 ug/1
Inactive Ingredients:
- Lactose Monohydrate
- Starch, Corn
- Povidone, Unspecified
- Magnesium Stearate /
Pharmaceutical Classes:
- Phosphodiesterase 4 Inhibitor [EPC]
- Phosphodiesterase 4 Inhibitors [MoA]
Related Products:
Based on records with the same trade name.- 0310-0095 Daliresp 500 ug/1 Oral Tablet by Astrazeneca Pharmaceuticals Lp
- 0456-0095 Daliresp 0.5 mg Oral Tablet by Forest Laboratories, Inc.
- 55154-4625 Daliresp 500 ug/1 Oral Tablet by Cardinal Health
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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.