NDC product
GUNA-DIUR
NDC 17089-260 · Guna spa
Key facts
| Product NDC | 17089-260 |
|---|---|
| Proprietary name | GUNA-DIUR |
| Nonproprietary name | amiloride - apis mellifera - berberis vulgaris fruit - hieracium pilosella flowering top - hydrochlorothiazide - solidago virgaurea flowering top - spironolactone - sus scrofa pituitary gland - |
| Substances | AMILORIDE, APIS MELLIFERA, BERBERIS VULGARIS FRUIT, HYDROCHLOROTHIAZIDE, SUS SCROFA PITUITARY GLAND, HIERACIUM PILOSELLA FLOWERING TOP, SOLIDAGO VIRGAUREA FLOWERING TOP, SPIRONOLACTONE |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Decreased Renal K+ Excretion [PE] and 7 more |
| Marketing start | May 23, 2006 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: