Epinephrine

Product NDC
71872-7304
Requested package NDC
71872-7304-1
11-digit product format
718727304
Labeler code
71872
Product ID
71872-7304_093312a8-528c-d515-e063-6394a90afd8f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Epinephrine
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
Medical Purchasing Solutions, LLC
Application
NDA211363
Marketing category
NDA
Marketing start
2023-01-30
Substance
EPINEPHRINE
Active strength
.1 mg/mL
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

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N211363-001EPINEPHRINEEPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-1584e616aacf4f…
2026-08-18 06:07:402026-07N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-1531067a03dcf5…
2025-08-23 18:47 UTC2025-08N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-156a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-1503ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-152680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-155bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15d8e5a09893c0…
2024-10-29 15:01 UTC2024-10N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-1579d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-151e350fbaab3a…
2024-05-31 18:47 UTC2024-05N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-158072bd15b7f6…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-156a51e52b5d6a…
2024-02-18 07:12 UTC2024-02N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-151c564ffb4f44…
2023-12-20 04:57 UTC2023-12N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-159b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-153f0d92c62455…
2023-05-13 08:27 UTC2023-05N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15053a50430f4f…
2023-01-26 05:58 UTC2023-01N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-153bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-153a93d1ddd44b…
2022-10-28 04:53 UTC2022-10N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15f41ea6bd6efb…
2022-09-29 23:25 UTC2022-09N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15e64feba35796…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06N211363-001EPINEPHRINE1MG/10ML (0.1MG/ML)SOLUTION / INTRAVENOUSRLD, RS2022-08-15a50c72e98297…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
EPINEPHRINE.1 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
YKH834O4BHInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
727373Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
093312af-6eed-1f4b-e063-6294a90a155dAvailable on FDA.report

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
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
f7046b89-2016-499a-adc6-78479172abc6Product name120230425
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
2686d634-e712-4007-8dbf-3d37c6c4d71fProduct name120181121
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
bd49bb86-2d32-4a7a-a594-eeda2e29af42Product name120180118
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
3becbe78-12d9-4ad2-9b4c-1e36f8d1303aProduct name120170815
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71872-7304-1Epinephrine1 in 1 BAGINJECTION11
71872-7304-1Epinephrine1 in 1 CARTONINJECTION11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71872-7304EPINEPHRINE INJECTION [MEDICAL PURCHASING SOLUTIONS, LLC]1Current NDC, 2 package rows20231103_093312af-6eed-1f4b-e063-6294a90a155d.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 · 7 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
EpinephrineEPINEPHRINEA-S Medication Solutions6e811e28-0199-4df7-a916-5940c632401d2026-07-13Warnings, Adverse reactionsExact identifier
application applno (NDA): 211363
application number: NDA211363
EpinephrineEPINEPHRINEREMEDYREPACK INC.0172280c-f7d6-4613-9dbd-f94d3ae5825a2026-06-08Warnings, Adverse reactionsExact identifier
application applno (NDA): 211363
application number: NDA211363
EPINEPHRINEEPINEPHRINEHenry Schein, Inc.3b1ac82f-6920-4e40-a77e-598398679f2d2025-10-31Warnings, Adverse reactionsExact identifier
application applno (NDA): 211363
application number: NDA211363
EpinephrineEPINEPHRINEProPharma Distribution3d728e53-92c2-114e-e063-6394a90ad4042025-08-28Warnings, Adverse reactionsExact identifier
application applno (NDA): 211363
application number: NDA211363
EpinephrineEPINEPHRINEInternational Medication Systems, Limitedf2b5f15b-8541-466a-a27a-ee57bc4aac672024-12-16Warnings, Adverse reactionsExact identifier
application applno (NDA): 211363
application number: NDA211363
EPINEPHRINEEPINEPHRINEHF Acquisition Co LLC, DBA HealthFirstf9c82678-5f4d-fded-e053-6394a90ac16d2024-01-22Warnings, Adverse reactionsExact identifier
application applno (NDA): 211363
application number: NDA211363
EpinephrineEPINEPHRINEMedical Purchasing Solutions, LLC093312af-6eed-1f4b-e063-6294a90a155d2023-11-02Warnings, Adverse reactionsExact identifier
application applno (NDA): 211363
application number: NDA211363
ndc (package): 71872-7304-1
ndc (product): 71872-7304
ndc11 (package): 71872730401

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
727373EPINEPHrine 1 MG in 10 ML Prefilled SyringePSN093312af-6eed-1f4b-e063-6294a90a155d1
72737310 ML epinephrine 0.1 MG/ML Prefilled SyringeSCD093312af-6eed-1f4b-e063-6294a90a155d1
727373epinephrine 1 MG per 10 ML Prefilled SyringeSY093312af-6eed-1f4b-e063-6294a90a155d1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71872-7304-1718727304011 CARTON in 1 BAG (71872-7304-1) / 1 SYRINGE in 1 CARTON / 10 mL in 1 SYRINGE1 carton2023-07-12NoNoCurrent