FDA.reportPublic FDA data

Formica Rufa

Product NDC
37662-0733
11-digit product format
376620733
Labeler code
37662
Product ID
37662-0733_e32972ed-96e0-73f4-e053-2a95a90a61da
Type
HUMAN OTC DRUG
Nonproprietary name
Formica Rufa
Dosage form
PELLET
Route
ORAL
Labeler
Hahnemann Laboratories, INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-07-06
Substance
FORMICA RUFA
Active strength
6 [hp_C]/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Formica Rufa
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
FORMICA RUFA6 [hp_C]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii55H0W83JO5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-0733-1Formica Rufa200 in 1 VIAL, GLASSPELLET2001
37662-0733-2Formica Rufa1200 in 1 BOTTLE, GLASSPELLET12001
37662-0733-3Formica Rufa4000 in 1 BOTTLE, GLASSPELLET40001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-0733FORMICA RUFA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 3 package rows20220708_e32972ed-96df-73f4-e053-2a95a90a61da.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-0733-137662073301200 PELLET in 1 VIAL, GLASS (37662-0733-1) 200 pellet2022-07-060000-00-00NoNoCurrent
37662-0733-2376620733021200 PELLET in 1 BOTTLE, GLASS (37662-0733-2) 1200 pellet2022-07-060000-00-00NoNoCurrent
37662-0733-3376620733034000 PELLET in 1 BOTTLE, GLASS (37662-0733-3) 4000 pellet2022-07-060000-00-00NoNoCurrent