NDC 54859-701
UrinD/S 5 ingredients tablet
On the label: Llorens Pharmaceutical International Division.
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Llorens Pharmaceutical International Division names for other drugs.
Recalls
- Sep 5, 2017 · Class II · Llorens Pharmaceutical Corp.
Superpotent Drug: Subpotent Drug. FDA analysis found this product to be Out of Specification for assay which could result in either Subpotent and/or Superpotent tablets.
Lots: Lots: 22811601, 22811602, Exp. 05/18; 202U1601 Exp. 11/18
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Methenamine, Sodium Phosphate, Monobasic, Monohydrate, Phenyl Salicylate, Methyl: every company that makes it
- Form
- tablet
- Strength
- 5 ingredients
- Approval
- Unapproved drug other
- On the market since
- May 1, 1999
- Package NDCs
54859-701-0454859-701-10- Official label
- DailyMed (National Library of Medicine), updated Jun 9, 2014
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