Formica Rufa

Product NDC
37662-0739
11-digit product format
376620739
Labeler code
37662
Product ID
37662-0739_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
1 [hp_M]/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 RUFA1 [hp_M]/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii55H0W83JO5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
37662-0739-1Formica Rufa200 in 1 VIAL, GLASSPELLET2001
37662-0739-2Formica Rufa500 in 1 VIAL, GLASSPELLET5001
37662-0739-3Formica Rufa3000 in 1 BOTTLE, GLASSPELLET30001
37662-0739-4Formica Rufa10000 in 1 BOTTLE, GLASSPELLET100001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
37662-0739FORMICA RUFA PELLET [HAHNEMANN LABORATORIES, INC.]1Current NDC, Legacy NDC, 4 package rows20220708_e32972ed-96df-73f4-e053-2a95a90a61da.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37662-0739-137662073901200 PELLET in 1 VIAL, GLASS (37662-0739-1) 200 pellet2022-07-060000-00-00NoNoCurrent
37662-0739-237662073902500 PELLET in 1 VIAL, GLASS (37662-0739-2) 500 pellet2022-07-060000-00-00NoNoCurrent
37662-0739-3376620739033000 PELLET in 1 BOTTLE, GLASS (37662-0739-3) 3000 pellet2022-07-060000-00-00NoNoCurrent
37662-0739-43766207390410000 PELLET in 1 BOTTLE, GLASS (37662-0739-4) 10000 pellet2022-07-060000-00-00NoNoCurrent