Register entryRepackager / relabeller

Nordic Pharma, Inc.

Data as of · How to read this entry

Registered sites
1
Active NDC listings
15
Live patents
0
Countries
1
Base
United States
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Nordic Pharma, Inc.1205 Westlakes Drive, Suite 275, Berwyn, Pennsylvania (PA) 19312, United States (USA)Labelling3011965331079843051
Catalogue

Drug listings by form and route

15

15 active NDC listings: 15 human prescription drug. By marketing category: ANDA 9, NDA 4, NDA AUTHORIZED GENERIC 2.

Dosage formNDCs
tablet7
injection, solution4
solution3
suspension1
RouteNDCs
oral7
intravenous6
intramuscular3
intracardiac2
ophthalmic2
subcutaneous2
Labeller name on the listingNDCs
nordic pharma, inc.15
Catalogue

Marketed products

15
BrandGeneric nameForm / routeNDC
ARSENIC TRIOXIDEArsenic Trioxideinjection, solution, intravenous69918-720ANDA
Desmopressin AcetateDesmopressin Acetatetablet, oral69918-101NDA
Desmopressin AcetateDesmopressin Acetatetablet, oral69918-201NDA
Desmopressin AcetateDesmopressin Acetatesolution, intravenous69918-899NDA
Desmopressin AcetateDesmopressin Acetatesolution, intravenous69918-901NDA
Isoproterenol HydrochlorideIsoproterenol Hydrochlorideinjection, solution, intracardiac, intramuscular, intravenous, subcutaneous69918-731ANDA
Isoproterenol HydrochlorideIsoproterenol Hydrochlorideinjection, solution, intracardiac, intramuscular, intravenous, subcutaneous69918-735ANDA
LamotrigineLamotriginetablet, oral69918-350ANDA
LamotrigineLamotriginetablet, oral69918-360ANDA
LamotrigineLamotriginetablet, oral69918-370ANDA
LamotrigineLamotriginetablet, oral69918-380ANDA
Succinylcholine ChlorideSuccinylcholine Chlorideinjection, solution, intramuscular, intravenous69918-700ANDA
Timoptic in OcudoseTimolol Maleatesolution, ophthalmic69918-601ANDA
Tranexamic AcidTranexamic Acidtablet, oral69918-301NDA AUTHORIZED GENERIC
neomycin sulfate, polymyxin b sulfate and dexamethasoneneomycin sulfate, polymyxin b sulfate and dexamethasonesuspension, ophthalmic69918-515NDA AUTHORIZED GENERIC
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Common questions

Is Nordic Pharma, Inc. FDA approved?
Nordic Pharma, Inc. 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 Nordic Pharma, Inc.'s registered sites?
The FDA register lists Berwyn, PA. Registered operations: labelling.
What drugs does Nordic Pharma, Inc. make?
15 products are listed under Nordic Pharma, Inc. in the openFDA NDC Directory, most often as tablet; injection, solution; 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.