FDA.reportPublic FDA data

EPINEPHRINE

Product NDC
51662-1222
11-digit product format
516621222
Labeler code
51662
Product ID
51662-1222_ef6a8b2a-010d-10dd-e053-2a95a90a1555
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
EPINEPHRINE
Dosage form
INJECTION
Route
SUBCUTANEOUS
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Application
NDA020800
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2018-09-14
Substance
EPINEPHRINE
Active strength
.15 mg/.15mL
Pharmacologic classes
Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Catecholamine [EPC], Catecholamines [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
EPINEPHRINE.15 mg/.15mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiYKH834O4BH
Rxcui1870225, 1870230

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0b4ec9ca-d305-43fc-88dd-7a510313efe0Product name120260105
bb209f42-a85f-4fee-9d3d-c9dded168625Product name120251208
49628fc7-2031-4c28-bd31-0ef3aa8f44a3Product name320251118
cbf85893-59ef-423f-87d4-a573c000a8b9Product name820250731
b5b1095b-40cd-8a9e-b111-502545045b07Product name420250325
e190029e-423b-473c-8e04-2ada59b5b711Product name120250314
e0031c74-3853-42bc-8e10-86dbbe83992eProduct name220231116
f7046b89-2016-499a-adc6-78479172abc6Product name120230425
2686d634-e712-4007-8dbf-3d37c6c4d71fProduct name120181121
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
bd49bb86-2d32-4a7a-a594-eeda2e29af42Product name120180118
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
3becbe78-12d9-4ad2-9b4c-1e36f8d1303aProduct name120170815

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51662-1222-12020-02-07C16284748780-19d75b9d0-6412-f424-e053-dadaa90a57ceEPINEPHRINE INJECTION, USP AUTO INJECTOR
51662-1222-12020-01-31C16284748780-19d75b9d0-6412-f424-e053-dadaa90a57ceEPINEPHRINE INJECTION, USP AUTO INJECTOR

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51662-1222-1EPINEPHRINE0.15 mL in 1 SYRINGE, GLASSINJECTION0.157
51662-1222-1EPINEPHRINE1 in 1 CASEINJECTION17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51662-1222EPINEPHRINE INJECTION [HF ACQUISITION CO LLC, DBA HEALTHFIRST]7Current NDC, Legacy NDC, 2 package rows20221211_75dbc3f5-9caf-9f55-e053-2a91aa0a4719.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1870225EPINEPHrine (generic for Adrenaclick) 0.15 MG in 0.15 ML Auto-InjectorPSN75dbc3f5-9caf-9f55-e053-2a91aa0a47197
1870230EPINEPHrine (generic for Adrenaclick) 0.3 MG in 0.3 ML Auto-InjectorPSN75dbc3f5-9caf-9f55-e053-2a91aa0a47197
1870225NDA020800 0.15 ML epinephrine 1 MG/ML Auto-InjectorSCD75dbc3f5-9caf-9f55-e053-2a91aa0a47197
1870230NDA020800 0.3 ML epinephrine 1 MG/ML Auto-InjectorSCD75dbc3f5-9caf-9f55-e053-2a91aa0a47197
1870225epinephrine (generic for Adrenaclick) 0.15 MG per 0.15 ML Auto-InjectorSY75dbc3f5-9caf-9f55-e053-2a91aa0a47197
1870230epinephrine (generic for Adrenaclick) 0.3 MG per 0.3 ML Auto-InjectorSY75dbc3f5-9caf-9f55-e053-2a91aa0a47197

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
51662-1222-1516621222011 SYRINGE, GLASS in 1 CASE (51662-1222-1) / .15 mL in 1 SYRINGE, GLASS2018-09-140000-00-00NoNoCurrent