Register entry

SOLA Pharmaceuticals, LLC

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Registered sites
0
Active NDC listings
36
Labeller names
3
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

36

36 active NDC listings: 26 human prescription drug, 10 human otc drug. By marketing category: ANDA 26, OTC MONOGRAPH DRUG 8, NDA 2.

Dosage formNDCs
patch7
injection4
injection, solution4
solution/ drops4
tablet4
solution3
tablet, film coated3
capsule2
capsule, delayed release2
gel2
tablet, delayed release1
RouteNDCs
oral12
topical11
intramuscular5
ophthalmic5
intravenous4
epidural2
infiltration2
perineural2
subcutaneous1
Labeller name on the listingNDCs
sola pharmaceuticals, llc24
sola pharmaceuticals9
sola pharmaceuticals3
Catalogue

Marketed products

36
BrandGeneric nameForm / routeNDC
BACLOFENBACLOFENtablet, oral70512-782ANDA
COXANTOoxaprozincapsule, oral70512-814NDA
Cabergolinecabergolinetablet, oral70512-860ANDA
CapsimideCapsaicin 0.025% Topical Patchpatch, topical70512-016OTC MONOGRAPH DRUG
CyanocobalaminCyanocobalamininjection, intramuscular, subcutaneous70512-840ANDA
Cyclobenzaprine HydrochlorideCyclobenzaprine Hydrochloridetablet, film coated, oral70512-872ANDA
Diclofenac Potassiumdiclofenac potassiumtablet, film coated, oral70512-750ANDA
Diclofenac Potassiumdiclofenac potassiumtablet, film coated, oral70512-900ANDA
Diclofenac SodiumDiclofenac Sodium 1%gel, topical70512-106ANDA
Diclofenac SodiumDiclofenac Sodiumtablet, delayed release, oral70512-784ANDA
Diclofenac SodiumDiclofenac Sodiumsolution, topical70512-810ANDA
Diclofenac Sodium 1.5%Diclofenac Sodium Topicalsolution, topical70512-038ANDA
Dimethyl FumarateDimethyl Fumaratecapsule, delayed release, oral70512-852ANDA
Dimethyl FumarateDimethyl Fumaratecapsule, delayed release, oral70512-853ANDA
Ibuprofenibuprofentablet, oral70512-780ANDA
Ibuprofenibuprofentablet, oral70512-794ANDA
Ketorolac Tromethamineketorolac tromethaminesolution, ophthalmic70512-790ANDA
Ketorolac TromethamineKetorolac Tromethamineinjection, intramuscular, intravenous70512-842ANDA
Ketorolac TromethamineKetorolac Tromethamineinjection, intramuscular, intravenous70512-843ANDA
Ketorolac TromethamineKetorolac Tromethamineinjection, intramuscular, intravenous70512-844ANDA
LenzaPro FlexLidocaine/Mentholpatch, topical70512-013OTC MONOGRAPH DRUG
LidaFlexLidocainepatch, topical70512-012OTC MONOGRAPH DRUG
Lidocaine 4% PatchLidocaine 4%patch, topical70512-014OTC MONOGRAPH DRUG
Lidocaine 4% PatchLidocaine 4%patch, topical70512-812OTC MONOGRAPH DRUG
Neuracin Topical GelNeuracin Topical Analgesic Gelgel, topical70512-104OTC MONOGRAPH DRUG
OfloxacinOfloxacin Ophthalmic Solution USP, 0.3%solution/ drops, ophthalmic70512-793ANDA
Olopatadine HclOlopatadine Hclsolution/ drops, ophthalmic70512-520ANDA
OxaprozinOxaprozincapsule, oral70512-787NDA
Phenylephrine HydrochloridePhenylephrine Hydrochloridesolution/ drops, ophthalmic70512-865ANDA
Phenylephrine HydrochloridePhenylephrine Hydrochloridesolution/ drops, ophthalmic70512-866ANDA
ROPIVACAINE HYDROCHLORIDEROPIVACAINE HYDROCHLORIDEinjection, solution, epidural, infiltration, perineural70512-797ANDA
ROPIVACAINE HYDROCHLORIDEROPIVACAINE HYDROCHLORIDEinjection, solution, epidural, infiltration, perineural70512-798ANDA
Sodium ChlorideSodium Chlorideinjection, solution, intravenous70512-841ANDA
SynoFlex PatchSynoFlex Patchpatch, topical70512-015OTC MONOGRAPH DRUG
TriceptinLidocaine / Menthol / Methyl Salicylatepatch, topical70512-017OTC MONOGRAPH DRUG
carboprost tromethaminecarboprost tromethamineinjection, solution, intramuscular70512-859ANDA
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Other companies listing ketorolac tromethamine

Enquiry

Common questions

Is SOLA Pharmaceuticals, LLC FDA approved?
SOLA Pharmaceuticals, LLC holds no registered establishment of its own; 36 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does SOLA Pharmaceuticals, LLC make?
36 products are listed under SOLA Pharmaceuticals, LLC in the openFDA NDC Directory, most often as patch; injection; injection, solution. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.