0574-0292 : Amiloride Hydrochloride 5 mg Oral Tablet
NDC: | 0574-0292 |
Labeler: | Paddock Laboratories, LLC |
Product Type: | Human Prescription Drug |
Drug Name: | Amiloride Hydrocloride |
Dosage Form: | Oral Tablet |
Application #: | NDA018200 |
Rev. Date: |
Appearance:
Markings: | P291 |
Shapes: |
Diamond (4 sides) |
Colors: |
White /
Yellow |
Size (mm): | 10 |
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:
- 0574-0292-01: 100 TABLET IN 1 BOTTLE (0574‑0292‑01)
Active Ingredients:
- Amiloride Hydrochloride
Dosage Strength:
- 5 mg
Inactive Ingredients:
- Lactose
- Magnesium Stearate
Pharmaceutical Classes:
- Decreased Renal K+ Excretion [PE]
- Increased Diuresis [PE]
- Potassium-sparing Diuretic [EPC]
Related Products:
Based on records with the same trade name.- 0179-0230 Amiloride Hydrocloride 5 mg Oral Tablet by Kaiser Foundation Hospitals
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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.