Sodum Acetate

Product NDC: 0517-5023
11-digit product format: 005175023
Labeler code: 0517
Product ID: 0517-5023_7da099a7-b1ba-4a93-b72a-75eb5f45db23
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Sodium Acetate
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Route: INTRAVENOUS
Labeler: American Regent, Inc.
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 1990-09-30
Marketing end: 0000-00-00
Substance: SODIUM ACETATE ANHYDROUS
Active strength: 328 mg/mL
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0517-5023-25	2024-12-17	C162847	48780-1	f386c649-dc33-0266-e053-dadaa90a7c1a	b619ee23-26ca-48c8-be40-7911f575e43d
0517-5023-25	2023-01-30	C162847	48780-1	f386c649-dc33-0266-e053-dadaa90a7c1a	b619ee23-26ca-48c8-be40-7911f575e43d

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0517-5023-25	ML - Milliliter	0517-5023	474badb4-e593-4d55-a990-90cfa044a25c	1	2014-10-03

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
NVG71ZZ7P0	SODIUM ACETATE ANHYDROUS	127-09-3	SODIUM ACETATE ANHYDROUS
4550K0SC9B	SODIUM ACETATE	6131-90-4	Sodium Acetate

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
0517-5023-25	00517502325	25 VIAL, SINGLE-DOSE in 1 TRAY (0517-5023-25) > 50 mL in 1 VIAL, SINGLE-DOSE	1990-09-30	0000-00-00	No	No	Current