NDC Code(s) : 76112-520-30
Packager : Jubilant HollisterStier General Partnership

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Pentetic Acidpentetic acid INJECTION
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:76112-520
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PENTETIC ACID(UNII: 7A314HQM0I)
(PENTETIC ACID - UNII:7A314HQM0I) 		PENTETIC ACID20 mg
Inactive Ingredients
Ingredient Name Strength
AMINOBENZOIC ACID(UNII: TL2TJE8QTX)5 mg in 1 1
CALCIUM CHLORIDE(UNII: M4I0D6VV5M)3.73 mg in 1 1
STANNOUS CHLORIDE(UNII: 1BQV3749L5)0.25 mg in 1 1
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:76112-520-3030 in 1 KIT Type 0: Not a Combination Product29/12/1989
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT NDA018511 12/29/1989

PRINCIPAL DISPLAY PANEL

DTPA 30 countDTPA 30 count