Pancreas Argentum

Product NDC
48951-8000
Requested package NDC
48951-8000-1
11-digit product format
489518000
Labeler code
48951
Product ID
48951-8000_6d08eda2-6b54-0a62-e053-2a91aa0ae4c3
Type
HUMAN OTC DRUG
Nonproprietary name
Pancreas Argentum
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
ECHINACEA ANGUSTIFOLIA; SUS SCROFA PANCREAS; SILVER
Active strength
3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage48951-800048951-8000-1IInactivated by FDA2026-10-05

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-8000-12026-01-29C16284748780-149896155-a213-586f-e063-e6dba90add90Pancreas Argentum

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8000-1Pancreas Argentum1 mL in 1 AMPULELIQUID13
48951-8000-1Pancreas Argentum10 in 1 BOXLIQUID103

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ECHINACEA ANGUSTIFOLIAACTIVE INGREDIENTVB06AV5US8PANCREAS ARGENTUM LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE INGREDIENT3M4G523W1GPANCREAS ARGENTUM LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA PANCREASACTIVE INGREDIENT9Y3J3362RYPANCREAS ARGENTUM LIQUID [URIEL PHARMACY INC.]1
ECHINACEA ANGUSTIFOLIAACTIVE MOIETYVB06AV5US8PANCREAS ARGENTUM LIQUID [URIEL PHARMACY INC.]1
SILVERACTIVE MOIETY3M4G523W1GPANCREAS ARGENTUM LIQUID [URIEL PHARMACY INC.]1
SUS SCROFA PANCREASACTIVE MOIETY9Y3J3362RYPANCREAS ARGENTUM LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XPANCREAS ARGENTUM LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RPANCREAS ARGENTUM LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8000PANCREAS ARGENTUM LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 2 package rows20180525_bca2da45-c39f-4875-b2ea-ce532e7242b7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8000-14895180000110 AMPULE in 1 BOX (48951-8000-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent