FDA.reportPublic FDA data

Interferon

Product NDC
43857-0218
11-digit product format
438570218
Labeler code
43857
Product ID
43857-0218_190e45f2-2db3-4be7-af16-ec33607fbfdd
Type
HUMAN OTC DRUG
Nonproprietary name
Interferon (Suis)
Dosage form
LIQUID
Route
ORAL
Labeler
BioActive Nutritional
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-09-23
Marketing end
0000-00-00
Substance
INTERFERON .GAMMA. PORCINE RECOMBINANT
Active strength
6 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct43857-0218DDiscontinued by firm2026-07-31
excluded packagepackage43857-021843857-0218-1DDiscontinued by firm2026-07-31

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43857-0218-12023-06-08C16284748780-19d75b9d0-2b1b-f424-e053-dadaa90a57ceDRUG FACTS:
43857-0218-12020-01-31C16284748780-19d75b9d0-2b1b-f424-e053-dadaa90a57ceDRUG FACTS:

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
INTERFERON .GAMMA. PORCINE RECOMBINANTACTIVE INGREDIENT69404B0LO7INTERFERON (INTERFERON (SUIS)) LIQUID [BIOACTIVE NUTRITIONAL]1
INTERFERON .GAMMA. PORCINE RECOMBINANTACTIVE MOIETY69404B0LO7INTERFERON (INTERFERON (SUIS)) LIQUID [BIOACTIVE NUTRITIONAL]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MINTERFERON (INTERFERON (SUIS)) LIQUID [BIOACTIVE NUTRITIONAL]1
WATERINACTIVE INGREDIENT059QF0KO0RINTERFERON (INTERFERON (SUIS)) LIQUID [BIOACTIVE NUTRITIONAL]1