Država: Sjedinjene Američke Države
Jezik: engleski
Izvor: NLM (National Library of Medicine)
OMEPRAZOLE SODIUM (UNII: KV03YZ6QLW) (OMEPRAZOLE - UNII:KG60484QX9)
AX Pharmaceutical Corp
OMEPRAZOLE SODIUM
OMEPRAZOLE 247.5 g in 250 g
NOT APPLICABLE
Bulk Ingredient For Animal Drug Compounding
AX PHARMACEUTICAL CORP- OMEPRAZOLE SODIUM POWDER AX PHARMACEUTICAL CORP ---------- AX PHARMACEUTICAL CORP omeprazole sodium powder AX Pharmaceutical Corp PRODUCT INFORMATION PRODUCT T YPE BULK INGREDIENT ITE M CODE (SOURCE ) NDC:6 2157-48 4 ROUTE OF ADMINISTRATION NOT APPLICABLE ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH O MEPRAZO LE SO DIUM (UNII: KV0 3YZ6 QLW) (OMEPRAZOLE - UNII:KG6 0 48 4QX9 ) OMEPRAZOLE 247.5 g in 250 g INACTIVE INGREDIENTS INGREDIENT NAME STRE NG TH WATER (UNII: 0 59 QF0 KO0 R) PRODUCT CHARACTERISTICS COLOR white S CORE S HAP E S IZ E FLAVOR IMPRINT CODE CONTAINS PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:6 2157-48 4-0 1 250 g in 1 JAR 0 8 /25/20 17 MARKETING INFORMATION MARKE TING CATE GORY APPLICATION NUMBE R OR MONOGRAPH CITA TIO N MARKE TING START DATE MARKE TING END DATE bulk ingredient fo r animal drug c o mpo unding 0 8 /25/20 17 LABELER - AX Pharmaceutical Corp (202924858) ESTABLISHMENT NAME AD D RE S S ID/FEI BUSINE SS OPE RATIONS AX Pharmaceutical Co rp 20 29 248 58 repack(6 2157-48 4) , relabel(6 2157-48 4) Revised: 8/2017 Pročitajte cijeli dokument