Valsts: Amerikas Savienotās Valstis
Valoda: angļu
Klimata pārmaiņas: NLM (National Library of Medicine)
CYCLOSPORINE (UNII: 83HN0GTJ6D) (CYCLOSPORINE - UNII:83HN0GTJ6D)
Imprimis NJOF, LLC
OPHTHALMIC
PRESCRIPTION DRUG
unapproved drug other
CYCLOSPORINE/CHONDROITIN PF- CYCLOSPORINE/CHONDROITIN SULFATE PF EMULSION IMPRIMIS NJOF, LLC _Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been_ _approved by FDA. For further information about unapproved drugs, click here._ ---------- STORE AT 20° TO 25° C (68° TO 77° F) CYCLOSPORINE/CHONDROITIN PF cyclosporine/chondroitin sulfate pf emulsion PRODUCT INFORMATION PRODUCT T YPE HUMAN PRESCRIPTION DRUG ITE M CODE (SOURCE ) NDC:7138 4-514 ROUTE OF ADMINISTRATION OPHTHALMIC ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH CYCLO SPO RINE (UNII: 8 3HN0 GTJ6 D) (CYCLOSPORINE - UNII:8 3HN0 GTJ6 D) CYCLOSPORINE 1 mg in 1 mL PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:7138 4-514- 0 5 5.5 mL in 1 BOTTLE, DROPPER; Type 0 : No t a Co mbinatio n Pro duc t 0 7/0 1/20 18 MARKETING INFORMATION MARKE TING CATE GORY APPLICATION NUMBE R OR MONOGRAPH CITATION MARKE TING START DATE MARKE TING END DATE unappro ved drug o ther 0 7/0 1/20 18 Imprimis NJOF, LLC LABELER - Imprimis NJOF, LLC (080431967) Revised: 2/2020 Izlasiet visu dokumentu