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Willow Birch Pharma, LLC

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Registered sites
1
Active NDC listings
83
Labeller names
7
Live patents
0
Countries
1
Base
United States
Authorisation

Registered operations

Relabelling1Repackaging1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Willow Birch Pharma, LLC447 County Road 303 Ste B, Taylor, Mississippi (MS) 38673, United States (USA)Relabelling, Repackaging3009864247617153924
Catalogue

Drug listings by form and route

83

83 active NDC listings: 82 bulk ingredient, 1 drug for further processing. By marketing category: BULK INGREDIENT 53, BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING 29, DRUG FOR FURTHER PROCESSING 1.

Dosage formNDCs
powder78
crystal3
gel1
syrup1
RouteNDCs
Labeller name on the listingNDCs
willow birch pharma, llc49
willow birch pharma, inc.19
willow birch pharma, llc.9
willow birch pharma, inc3
willow birch pharma1
willow birch pharma, inc1
willow birch pharma, inc.1
Catalogue

Marketed products

83
BrandGeneric nameForm / routeNDC
-Acetylcysteinepowder10695-066BULK INGREDIENT
-Allopurinolpowder10695-332BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Alpha-Lipoic Acidpowder10695-310BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Amantadine Hydrochloridepowder10695-014BULK INGREDIENT
-Ascorbic Acidpowder10695-126BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Atorvastatin Calciumpowder10695-166BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Biotinpowder10695-306BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Biotinpowder10695-325BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Budesonidepowder10695-124BULK INGREDIENT
-Bupivacaine HCLpowder10695-038BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Bupropion Hydrochloridepowder10695-170BULK INGREDIENT
-Calcium Chloride Dihydratecrystal10695-339BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Cetirizine Hydrochloridepowder10695-143BULK INGREDIENT
-Choline Chloridepowder10695-335BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Cyanocobalaminpowder10695-172BULK INGREDIENT
-Cyclobenzaprine HCLpowder10695-117BULK INGREDIENT
-Cyclophosphamidepowder10695-340BULK INGREDIENT
-Dexpanthenolsyrup10695-317BULK INGREDIENT
-Dried Aluminum Hydroxide Gelgel10695-164DRUG FOR FURTHER PROCESSING
-Dutasteridepowder10695-152BULK INGREDIENT
-Enclomiphene Citratepowder10695-307BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Escitalopram Oxalatepowder10695-177BULK INGREDIENT
-Ezetimibepowder10695-318BULK INGREDIENT
-Finasteridepowder10695-151BULK INGREDIENT
-Fluoxetinepowder10695-173BULK INGREDIENT
-Gabapentinpowder10695-196BULK INGREDIENT
-Glutathionepowder10695-331BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Glycinepowder10695-326BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Hydroxocobalaminpowder10695-341BULK INGREDIENT
-Inositolpowder10695-249BULK INGREDIENT
-Ivermectinpowder10695-052BULK INGREDIENT
-Ketoconazolepowder10695-141BULK INGREDIENT
-Ketoconazolepowder10695-304BULK INGREDIENT
-L-Argininepowder10695-320BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-L-Cysteine Hydrochloride Monohydratepowder10695-128BULK INGREDIENT
-Leucovorin Calciumpowder10695-001BULK INGREDIENT
-Levamisole HCLpowder10695-031BULK INGREDIENT
-Levocarnitinepowder10695-333BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Marbofloxacinpowder10695-144BULK INGREDIENT
-Melatoninpowder10695-315BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Metformin HCLpowder10695-199BULK INGREDIENT
-Methazolamidepowder10695-171BULK INGREDIENT
-Methioninepowder10695-336BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Methylcobalaminpowder10695-174BULK INGREDIENT
-Methylprednisolone Acetatepowder10695-041BULK INGREDIENT
-Minoxidilpowder10695-149BULK INGREDIENT
-Minoxidilpowder10695-327BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Mometasone Furoatepowder10695-111BULK INGREDIENT
-NALTREXONE HYDROCHLORIDEpowder10695-130BULK INGREDIENT
-Naltrexone HCLpowder10695-114BULK INGREDIENT
-Naltrexone Hydrochloridepowder10695-115BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Naltrexone Hydrochloridepowder10695-129BULK INGREDIENT
-Naltrexone Hydrochloridepowder10695-131BULK INGREDIENT
-Naltrexone Hydrochloridepowder10695-132BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Naltrexone Hydrochloride Dihydratepowder10695-167BULK INGREDIENT
-Niacinamidepowder10695-308BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Papaverine HCLpowder10695-116BULK INGREDIENT
-Phenylephrine HCLpowder10695-036BULK INGREDIENT
-Potassium Chloridecrystal10695-328BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Pyridoxine Hydrochloridepowder10695-334BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Riboflavin 5-Phosphate Sodiumpowder10695-330BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Rifaximinpowder10695-011BULK INGREDIENT
-Rosuvastatin Calciumpowder10695-118BULK INGREDIENT
-Rosuvastatin Calciumpowder10695-337BULK INGREDIENT
-Sermorelin Acetatepowder10695-200BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Sildenafil Citratepowder10695-017BULK INGREDIENT
-Sildenafil Citratepowder10695-329BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Sucralfatepowder10695-162BULK INGREDIENT
-TadalafilUSPpowder10695-175BULK INGREDIENT
-Telmisartanpowder10695-139BULK INGREDIENT
-Tetracainepowder10695-087BULK INGREDIENT
-Thiamine HCLpowder10695-305BULK INGREDIENT
-Tobramycin Sulfatepowder10695-008BULK INGREDIENT
-Topiramatepowder10695-119BULK INGREDIENT
-Topiramatepowder10695-311BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Trisodium Citrate Dihydratepowder10695-321BULK INGREDIENT
-Trisodium Citrate Dihydratepowder10695-338BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Vancomycin HCLpowder10695-039BULK INGREDIENT
-Vardenafil HCL Trihydratepowder10695-312BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Vardenafil Hydrochloridepowder10695-120BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-Vardenafil Hydrochloridepowder10695-122BULK INGREDIENT
-Vardenafil Hydrochloridepowder10695-123BULK INGREDIENT
-Zinc Sulfate Monohydratecrystal10695-163BULK INGREDIENT
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Enquiry

Common questions

Is Willow Birch Pharma, LLC FDA approved?
Willow Birch Pharma, LLC holds 1 FDA-registered establishment in the United States. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Willow Birch Pharma, LLC's registered sites?
The FDA register lists Taylor, MS. Registered operations: relabelling, repackaging.
What drugs does Willow Birch Pharma, LLC make?
83 products are listed under Willow Birch Pharma, LLC in the openFDA NDC Directory, most often as powder; crystal; gel. 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.