FDA.reportPublic FDA data

Albuterol

Product NDC
71205-898
11-digit product format
712050898
Labeler code
71205
Product ID
71205-898_f5ac6375-7f17-4d27-b13a-b44e73281838
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
albuterol
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA207046
Marketing category
ANDA
Marketing start
2018-06-29
Substance
ALBUTEROL SULFATE
Active strength
2 mg/1
Pharmacologic classes
Adrenergic beta2-Agonists [MoA], beta2-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
Albuterol
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ALBUTEROL SULFATE2 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii021SEF3731
Rxcui197316, 197318

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
26005090-31a1-441d-920b-db3101a55d53Product name320250221
1c39b897-7219-42a1-9f3a-ec86cfd7b04bProduct name320250218
0a278166-c8aa-41b6-b4a5-6ac332bde76aProduct name120230718
c76bcd0f-25eb-471e-b970-1956c95c26c5Product name120230425
36390b75-5438-47d3-af60-732a654e9025Product name220220110
387afa72-0c5a-0d6b-ee2c-60c3506659e8Product name620210518
1b8ea3ec-88bd-98ea-c961-00ae340b5b14Product name220200220
3aa5a017-61e9-0c89-adef-13e7964d22f0Product name320171208
c3c27a99-b8bc-4955-841c-26555f58ee7eProduct name120150421
bc98cf6f-a973-7162-5e30-0e7dd8c56bc3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71205-898-00Albuterol100 in 1 BOTTLETABLET1003
71205-898-11Albuterol1000 in 1 BOTTLETABLET10003
71205-898-30Albuterol30 in 1 BOTTLETABLET303
71205-898-55Albuterol500 in 1 BOTTLETABLET5003
71205-898-60Albuterol60 in 1 BOTTLETABLET603
71205-898-90Albuterol90 in 1 BOTTLETABLET903

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71205-898-00EA - Each71205-89811c47375-e7aa-4a7c-887b-56ea6b4c24a912021-09-07
71205-898-11EA - Each71205-898e55f86fa-5665-4c1b-b0c1-cb00803292a712021-09-07
71205-898-30EA - Each71205-898467a4a16-30ac-4b06-a2e8-6b65bffef42312021-09-07
71205-898-55EA - Each71205-89854d291a9-dc7d-4204-a514-76b8b035f2ce12021-09-07
71205-898-60EA - Each71205-8985ebfcc66-cfcf-4570-a539-ceb474b3c79612021-09-07
71205-898-90EA - Each71205-89827a9893a-ee34-4b75-b8db-8f278411f9c512021-09-07

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71205-898ALBUTEROL TABLET [PROFICIENT RX LP]3Current NDC, Legacy NDC, 6 package rows20220415_895dff1c-d21c-4470-b021-a5b68364c1ec.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197316albuterol 2 MG Oral TabletPSN895dff1c-d21c-4470-b021-a5b68364c1ec3
197318albuterol 4 MG Oral TabletPSN895dff1c-d21c-4470-b021-a5b68364c1ec3
197316albuterol 2 MG Oral TabletSCD895dff1c-d21c-4470-b021-a5b68364c1ec3
197318albuterol 4 MG Oral TabletSCD895dff1c-d21c-4470-b021-a5b68364c1ec3
197316albuterol 2 MG (as albuterol sulfate 2.4 MG) Oral TabletSY895dff1c-d21c-4470-b021-a5b68364c1ec3
197318albuterol 4 MG (as albuterol sulfate 4.8 MG) Oral TabletSY895dff1c-d21c-4470-b021-a5b68364c1ec3

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71205-898-0071205089800100 TABLET in 1 BOTTLE (71205-898-00) 100 tablet2021-07-300000-00-00NoNoCurrent
71205-898-11712050898111000 TABLET in 1 BOTTLE (71205-898-11) 1000 tablet2021-07-300000-00-00NoNoCurrent
71205-898-307120508983030 TABLET in 1 BOTTLE (71205-898-30) 30 tablet2021-07-300000-00-00NoNoCurrent
71205-898-5571205089855500 TABLET in 1 BOTTLE (71205-898-55) 500 tablet2021-07-300000-00-00NoNoCurrent
71205-898-607120508986060 TABLET in 1 BOTTLE (71205-898-60) 60 tablet2021-07-300000-00-00NoNoCurrent
71205-898-907120508989090 TABLET in 1 BOTTLE (71205-898-90) 90 tablet2021-07-300000-00-00NoNoCurrent