Země: Spojené státy
Jazyk: angličtina
Zdroj: NLM (National Library of Medicine)
PREDNISONE (UNII: VB0R961HZT) (PREDNISONE - UNII:VB0R961HZT)
Shertech Laboratories, LLC
PREDNISONE
PREDNISONE 50 mg in 50 mg
PRESCRIPTION DRUG
Contrast Allergy PreMed Pack TM consists of an administration card containing three Prednisone 50 mg tablets, USP, and one Diphenhydramine Hydrochloride 50 mg capsule, USP, for oral administration.
unapproved drug other
CONTRAST ALLERGY PREMED PACK- PREDNISONE, DIPHENHYDRAMINE SHERTECH LABORATORIES, 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._ ---------- CONTRAST ALLERGY PREMED PACK DESCRIPTION Contrast Allergy PreMed Pack consists of an administration card containing three Prednisone 50 mg tablets, USP, and one Diphenhydramine Hydrochloride 50 mg capsule, USP, for oral administration. CONTRAST ALLERGY PREMED PACK NDC 16129-101-01 double therapy Contrast Allergy PreMed Pack PREDNISONE DIPHENHYDRAMINE BLISTER PACK CONTAINS: 3 PREDNISONE, USP, 50 mg Tablets; and 1 DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE, USP, 50 mg Rx only TM TM TM CONTRAST ALLERGY PREMED PACK prednisone, diphenhydramine kit PRODUCT INFORMATION PRODUCT T YPE HUMAN PRESCRIPTION DRUG ITE M CODE (SOURCE ) NDC:16 129 -10 1 PACKAG ING # ITEM CODE PACKAGE DESCRIPTION MARKETING START DATE MARKETING END DATE 1 NDC:16 129 -10 1- 0 1 1 in 1 BLISTER PACK; Type 1: Co nvenience Kit o f Co - Pa c ka ge 0 9 /13/20 16 QUANTITY OF PARTS PART # PACKAGE QUANTITY TOTAL PRODUCT QUANTITY PA RT 1 3 PA RT 2 1 PART 1 OF 2 PREDNISONE prednisone tablet PRODUCT INFORMATION ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH PREDNISO NE (UNII: VB0 R9 6 1HZT) (PREDNISONE - UNII:VB0 R9 6 1HZT) PREDNISONE 50 mg in 50 mg PRODUCT CHARACTERISTICS COLOR white S CORE sco re with uneven pieces S HAP E ROUND S IZ E 10 mm FLAVOR IMPRINT CODE CONTAINS 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 PART 2 OF 2 DIPHENHYDRAMINE HYDROCHLORIDE diphenhydramine hydrochloride capsule PRODUCT INFORMATION ROUTE OF ADMINISTRATION ORAL ACTIVE INGREDIENT/ACTIVE MOIETY INGREDIENT NAME BASIS OF STRENGTH STRE NG TH DIPHENHYDRAMINE HYDRO CHLO RIDE (UNII: TC2D6 JAD40 ) (DIPHENHYDRAMINE - UNII:8 GTS8 2S8 3M) DIPHENHYDRAMINE HYD Přečtěte si celý dokument