69097-844 : Alfuzosin Hydrochloride Extended Release 10 mg Oral Tablet
NDC: | 69097-844 |
Labeler: | Cipla USA Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Alfuzosin Hydrochloride Extended Release |
Dosage Form: | Oral Tablet |
Application #: | ANDA090284 |
Rev. Date: |
Appearance:
Markings: | IG;302 |
Shapes: |
Round |
Colors: |
White |
Size (mm): | 9 |
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:
- 69097-844-02: 30 TABLET IN 1 BOTTLE (69097‑844‑02)
- 69097-844-05: 90 TABLET IN 1 BOTTLE (69097‑844‑05)
- 69097-844-07: 100 TABLET IN 1 BOTTLE (69097‑844‑07)
- 69097-844-12: 500 TABLET IN 1 BOTTLE (69097‑844‑12)
Active Ingredients:
- Alfuzosin Hydrochloride
Dosage Strength:
- 10 mg
Inactive Ingredients:
- Cellulose, Microcrystalline
- Guar Gum
- Hypromelloses
- Silicon Dioxide
- Magnesium Stearate
Pharmaceutical Classes:
- Adrenergic alpha-Antagonists [MoA]
- alpha-Adrenergic Blocker [EPC]
Related Products:
Based on records with the same trade name.- 69189-0304 Alfuzosin Hydrochloride Extended Release 10 mg Oral Tablet by Avera Mckennan Hospital
- 70934-961 Alfuzosin Hydrochloride Extended Release 10 mg Oral Tablet by Denton Pharma, Inc. Dba Northwind Pharmaceuticals
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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.