Medication Brand Names Beginning with ‘S’

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SABRIL (Vigabatrin)

SABRIL is indicated for the treatment of: Refractory Complex Partial Seizures as adjunctive therapy in patients >=10 years of age who have responded inadequately to several alternative treatments; Sabril is not indicated as a first line agent (1.1)…

Lundbeck LLC29 June 2016

SABRIL (Vigabatrin)

SABRIL is indicated for the treatment of: Refractory Complex Partial Seizures as adjunctive therapy in patients 2 years of age and older who have responded inadequately to several…

Lundbeck Pharmaceuticals LLC19 October 2020

Safyral (Drospirenone/ethinyl Estradiol/levomefolate Calcium and Levomefolate Calcium)

Safyral is an estrogen/progestin COC containing a folate, indicated for use by women to: Prevent pregnancy. (1.1) Raise folate levels in women who choose to use an oral…

Bayer HealthCare Pharmaceuticals Inc.8 August 2017

Saizen (Somatropin)

SAIZEN is a recombinant human growth hormone indicated for: Pediatric: Treatment of children with growth failure due to growth hormone deficiency (GHD) (1.1) Adult: Treatment of adults…

EMD Serono, Inc.7 April 2020

Salacyn (Salicylic Acid)

SALACYN(TM) 6%. is a topical aid in the removal of excessive keratin in hyperkeratotic skin disorders including verrucae, and the various ichthyoses (vulgaris, sex-linked and lamellar), keratosis palmaris and plantaris keratosis pilaris, pityriasis…

Stratus Pharamceuticals, Inc11 November 2010

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FDA Medwatch

Fusion Health and Vitality Issues Voluntary Nationwide Recall of Core Essential Nutrients and Immune Boost Sublingual Vitamin D3 Due to the Unapproved Use of a Food Additive and Unapproved Marketing Statements
Sun, 22 Nov 2020. Fusion Health and Vitality LLC is voluntarily recalling all 2020 Lots of CORE essential nutrients and Immune Boost Sublingual Vitamin D3. CORE has been found to contain an unapproved food additive, hordenine HCl, rendering it adulterated. Immune…
Fresenius Kabi Issues Voluntary Nationwide Recall of a Single Lot of Dexmedetomidine Hydrochloride Injection Due to Cross-Contamination of Lidocaine
Wed, 18 Nov 2020. Fresenius Kabi USA is voluntarily recalling a single lot of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg/50 mL (4 mcg /mL), 50 mL fill in a 50 mL vial. Fresenius Kabi initiated this recall due to a trace amount of lidocaine present…

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