Register entryRepackager / relabeller

Allegis Pharmaceuticals, Inc.

Data as of · How to read this entry

Registered sites
2
Active NDC listings
16
Labeller names
4
Live patents
0
Countries
1
Base
United States
Authorisation

Registered operations

Labelling2
Sites

Registered establishments

2
EstablishmentAddressRegistered forFEI / DUNS
Allegis Holdings LLC276 Nissan Parkway F100, Canton, Mississippi (MS) 39046, United States (USA)Labelling3023824887080556861
Allegis Pharmaceuticals, Inc.276 Nissan Parkway F100, Canton, Mississippi (MS) 39046, United States (USA)Labelling3007566601792272861
Catalogue

Drug listings by form and route

16

16 active NDC listings: 11 human prescription drug, 5 human otc drug. By marketing category: ANDA 5, OTC MONOGRAPH DRUG 5, UNAPPROVED DRUG OTHER 3, NDA AUTHORIZED GENERIC 2, NDA 1.

Dosage formNDCs
syrup4
capsule3
cream2
suspension2
for suspension1
lotion1
solution1
spray1
tablet1
RouteNDCs
oral10
topical6
Labeller name on the listingNDCs
allegis pharmaceuticals, llc10
allegis holdings llc2
allegis holdings, llc2
allegis pharmaceuticals, inc.2
Catalogue

Marketed products

16
BrandGeneric nameForm / routeNDC
AugmentinAmoxicillin and Clavulanate Potassiumfor suspension, oral71297-240NDA
Clotrimazole Topical Solution USP, 1%Clotrimazole Topical Solution USP, 1%solution, topical71297-030ANDA
HISTEXTRIPROLIDINE HYDROCHLORIDEsyrup, oral28595-802OTC MONOGRAPH DRUG
HISTEX PD Drops New FormulationTRIPROLIDINE HYDROCHLORIDEsyrup, oral28595-809OTC MONOGRAPH DRUG
HISTEX-DMDEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, and TRIPROLIDINE HYDROCHLORIDEsyrup, oral28595-804OTC MONOGRAPH DRUG
HISTEX-DM New FormulationDEXTROMETHORPHAN HBr, PSEUDOEPHEDRINE HCI, and TRIPROLIDINE HCIsyrup, oral28595-310OTC MONOGRAPH DRUG
HydrocortisoneHydrocortisone Lotionlotion, topical71297-010ANDA
Hydrocortisone Acetate CreamHydrocortisone Acetate Creamcream, topical28595-050ANDA
Hydrocortisone Acetate CreamHydrocortisone Acetate Creamcream, topical71297-241ANDA
MB CAPSmethenamine, sodium phosphate, monobasic, monohydrate, phenyl salicylate, methylene blue, and hyoscyamine sulfatecapsule, oral28595-299UNAPPROVED DRUG OTHER
Mag 440Megnesium Oxidetablet, oral28595-710OTC MONOGRAPH DRUG
NITROGLYCERIN LINGUALNitroglycerinspray, oral28595-120NDA AUTHORIZED GENERIC
OrudisKetoprofencapsule, oral28595-031ANDA
Spinosadspinosadsuspension, topical28595-570NDA AUTHORIZED GENERIC
URIMAR-T CAPSmethenamine, sodium phosphate, monobasic, monohydrate, phenyl salicylate, methylene blue, and hyoscyamine sulfatecapsule, oral28595-224UNAPPROVED DRUG OTHER
sulfacetamide sodium and sulfur Sodium Sulfacetamide - Sulfursulfacetamide sodium and sulfursuspension, topical28595-501UNAPPROVED DRUG OTHER
Neighbours

Registered in the same town

2
Compare

Comparable companies in United States

Enquiry

Common questions

Is Allegis Pharmaceuticals, Inc. FDA approved?
Allegis Pharmaceuticals, Inc. holds 2 FDA-registered establishments 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 Allegis Pharmaceuticals, Inc.'s registered sites?
The FDA register lists Canton, MS. Registered operations: labelling.
What drugs does Allegis Pharmaceuticals, Inc. make?
16 products are listed under Allegis Pharmaceuticals, Inc. in the openFDA NDC Directory, most often as syrup; capsule; cream. 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.