Ignatia

Product NDC
44911-0144
11-digit product format
449110144
Labeler code
44911
Product ID
44911-0144_a737812a-0898-4d52-b409-5806ce7c7f86
Type
HUMAN OTC DRUG
Nonproprietary name
Ignatia Amara
Dosage form
LIQUID
Route
ORAL
Labeler
Energique, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-05-08
Substance
STRYCHNOS IGNATII SEED
Active strength
200 [hp_C]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

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

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2020-06-10 20:45 UTC · source 2020-06-10excluded productproduct44911-0144IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…
2020-06-10 20:45 UTC · source 2020-06-10excluded packagepackage44911-014444911-0144-1IInactivated by FDAexcluded / ndc_excluded.zip9bebd1f3094a…5416666fcb17…

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
STRYCHNOS IGNATII SEED200 [hp_C]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1NM3M2487KInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
d6f7af5c-62d5-435b-854d-d43ede0350c9Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
EffectiveRelated label
2024-01-23DRUG FACTS:
2023-01-30DRUG FACTS:
2020-06-26DRUG FACTS:
2020-01-31DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0144-1Ignatia30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
STRYCHNOS IGNATII SEEDACTIVE INGREDIENT1NM3M2487KIGNATIA (IGNATIA AMARA) LIQUID [ENERGIQUE, INC.]1
STRYCHNOS IGNATII SEEDACTIVE MOIETY1NM3M2487KIGNATIA (IGNATIA AMARA) LIQUID [ENERGIQUE, INC.]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MIGNATIA (IGNATIA AMARA) LIQUID [ENERGIQUE, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RIGNATIA (IGNATIA AMARA) LIQUID [ENERGIQUE, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0144IGNATIA (IGNATIA AMARA) LIQUID [ENERGIQUE, INC.]4Current NDC, Legacy NDC, 1 package rows20240124_d6f7af5c-62d5-435b-854d-d43ede0350c9.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IgnatiaIGNATIA AMARAEnergique, Inc.d6f7af5c-62d5-435b-854d-d43ede0350c92024-01-23WarningsExact identifier
ndc (product): 44911-0144

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0144-14491101440130 mL in 1 BOTTLE, DROPPER (44911-0144-1) 30 ml2015-05-080000-00-00NoNoCurrent