Bambusa Formica

Product NDC
48951-2134
11-digit product format
489512134
Labeler code
48951
Product ID
48951-2134_b6af6fce-e027-254f-e053-2a95a90a324b
Type
HUMAN OTC DRUG
Nonproprietary name
Bambusa Formica
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
BAMBUSA VULGARIS WHOLE; VISCUM ALBUM FRUITING TOP; FORMICA RUFA; TIN; EQUISETUM ARVENSE TOP; BOS TAURUS EYE
Active strength
6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2134-1Bambusa Formica10 mL in 1 BOTTLE, DROPPERLIQUID103
48951-2134-1Bambusa Formica1 in 1 BAGLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2134BAMBUSA FORMICA LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 2 package rows20241010_92c2f4df-49e5-6345-e053-2a95a90a2531.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
48951-2134-1489512134011 BOTTLE, DROPPER in 1 BAG (48951-2134-1) > 10 mL in 1 BOTTLE, DROPPER2009-09-010000-00-00NoNoCurrent