Belladonna ex herba 3 Special Order

Product NDC
48951-2106
11-digit product format
489512106
Labeler code
48951
Product ID
48951-2106_6cb97027-6d85-bed5-e053-2a91aa0a77c1
Type
HUMAN OTC DRUG
Nonproprietary name
Belladonna ex herba 3 Special Order
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
ATROPA BELLADONNA
Active strength
3 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2106-1Belladonna ex herba 3 Special Order1 mL in 1 AMPULELIQUID12
48951-2106-1Belladonna ex herba 3 Special Order10 in 1 BOXLIQUID102

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0HBELLADONNA EX HERBA 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0HBELLADONNA EX HERBA 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XBELLADONNA EX HERBA 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RBELLADONNA EX HERBA 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2106BELLADONNA EX HERBA 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]2Legacy NDC, 2 package rows20180521_712a180c-ce95-4749-9cfa-b0521aca030d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-2106-14895121060110 AMPULE in 1 BOX (48951-2106-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent