Saluron
Name: Saluron
How Supplied
Saluron® Tablets, scored, 50 mg in bottles of 100.
NDC 54092-055-01
Store from 15° to 25°C (59° to 77°F).
Keep this and all medication out of the reach of children.
CAUTION: Federal law prohibits dispensing without prescription.
Saluron
hydroflumenthiazide tablet |
| Product Information | | Product Type | HUMAN PRESCRIPTION DRUG LABEL | Item Code (Source) | NDC:54092-055 | | Route of Administration | ORAL | DEA Schedule | | |
| Active Ingredient/Active Moiety | | Ingredient Name | Basis of Strength | Strength | | hydroflumethiazide (hydroflumethiazide) | hydroflumethiazide | 50 mg | |
| Inactive Ingredients | | Ingredient Name | Strength | | microcrystalline cellulose | | | lactose | | | magnesium stearate | | | colloidal silicon dioxide | | | sodium starch glycolate | | |
| Product Characteristics | | Color | WHITE | Score | 2 pieces | | Shape | ROUND | Size | 8mm | | Flavor | | Imprint Code | RPC;055 | | Contains | | | Coating | false | Symbol | false | |
| Packaging | | # | Item Code | Package Description | | 1 | NDC:54092-055-01 | 100 TABLET (100 TABLET) in 1 BOTTLE | |
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Revised: 07/2006 Shire
