Argentum 30

Product NDC: 48951-1083
11-digit product format: 489511083
Labeler code: 48951
Product ID: 48951-1083_9454d261-30d2-7fb8-e053-2a95a90ae699
Type: HUMAN OTC DRUG
Nonproprietary name: Argentum 30
Dosage form: LIQUID
Route: ORAL
Labeler: Uriel Pharmacy Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2009-09-01
Marketing end: 0000-00-00
Substance: SILVER
Active strength: 30 [hp_X]/mL
NDC exclude flag: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-1083-3	2025-01-30	C162847	48780-1	2cef2736-7d80-d83d-e063-dadaa90ab31f	Argentum 30

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
48951-1083-3	Argentum 30	60 mL in 1 BOTTLE, DROPPER	LIQUID	60		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
48951-1083	ARGENTUM 30 LIQUID [URIEL PHARMACY INC.]	2	Legacy NDC, 1 package rows	20191008_9453629a-a666-45ff-e053-2a95a90a9576.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
48951-1083-3	48951108303	60 mL in 1 BOTTLE, DROPPER (48951-1083-3)	60 ml	2009-09-01	0000-00-00	No	No	Current