NDC 76112-520-30
API & Excipient Details

Pentetic Acid marketed by Jubilant HollisterStier General Partnership under NDC Code 76112-520-30

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

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PENTETIC ACID(UNII: 7A314HQM0I) (PENTETIC ACID - UNII:7A314HQM0I)	PENTETIC ACID	20 mg

Ingredient Name	Strength
Inactive Ingredients
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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:76112-520-30	30 in 1 KIT Type 0: Not a Combination Product	29/12/1989

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT	NDA018511	12/29/1989

PRINCIPAL DISPLAY PANEL

DTPA 30 count

DTPA 30 count

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