Country: United States
Language: English
Source: NLM (National Library of Medicine)
ALENDRONATE SODIUM (UNII: 2UY4M2U3RA) (ALENDRONIC ACID - UNII:X1J18R4W8P)
AX Pharmaceutical Corp
ALENDRONATE SODIUM
ALENDRONIC ACID 99 g in 100 g
NOT APPLICABLE
Bulk Ingredient For Animal Drug Compounding
AX PHARMACEUTICAL CORP- ALENDRONATE SODIUM TRIHYDRATE POWDER AX PHARMACEUTICAL CORP ---------- AX PHARMACEUTICAL CORP AX Pharmaceutical Corp alendronate sodium trihydrate powder PRODUCT INFORMATION PRODUCT T YPE BULK INGREDIENT ITE M CODE (SOURCE ) NDC:6 2157-445 ROUTE OF ADMINISTRATION NOT APPLICABLE ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH ALENDRO NATE SO DIUM (UNII: 2UY4M2U3RA) (ALENDRONIC ACID - UNII:X1J18 R4W8 P) ALENDRONIC ACID 9 9 g in 10 0 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 2157-445-0 1 10 0 g in 1 JAR 0 8 /11/20 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 /11/20 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 pack(6 2157-445) , relabel(6 2157-445) Revised: 8/2017 Read the complete document