arformoterol tartrate

Generic: arformoterol tartrate

Labeler: lupin pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name arformoterol tartrate
Generic Name arformoterol tartrate
Labeler lupin pharmaceuticals, inc.
Dosage Form SOLUTION
Routes
RESPIRATORY (INHALATION)
Active Ingredients

arformoterol tartrate 15 ug/2mL

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 70748-175
Product ID 70748-175_65d81c00-8791-4937-8e25-4abfc9790e4b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA213068
Listing Expiration 2026-12-31
Marketing Start 2022-07-27

Pharmacologic Class

Classes
adrenergic beta2-agonists [moa] beta2-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70748175
Hyphenated Format 70748-175

Supplemental Identifiers

RxCUI
668956
UPC
0370748175019
UNII
5P8VJ2I235

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name arformoterol tartrate (source: ndc)
Generic Name arformoterol tartrate (source: ndc)
Application Number ANDA213068 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 15 ug/2mL
source: ndc
Packaging
  • 30 POUCH in 1 CARTON (70748-175-30) / 1 VIAL, SINGLE-DOSE in 1 POUCH / 2 mL in 1 VIAL, SINGLE-DOSE
  • 60 POUCH in 1 CARTON (70748-175-60) / 1 VIAL, SINGLE-DOSE in 1 POUCH / 2 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (2)

70748-175-30 30 POUCH in 1 CARTON (70748-175-30) / 1 VIAL, SINGLE-DOSE in 1 POUCH / 2 mL in 1 VIAL, SINGLE-DOSE 70748-175-60 60 POUCH in 1 CARTON (70748-175-60) / 1 VIAL, SINGLE-DOSE in 1 POUCH / 2 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

arformoterol tartrate (15 ug/2mL)

Linked Drug Pages (1)

Arformoterol tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "65d81c00-8791-4937-8e25-4abfc9790e4b", "openfda": {"upc": ["0370748175019"], "unii": ["5P8VJ2I235"], "rxcui": ["668956"], "spl_set_id": ["cf1f2d1b-0455-4113-9647-507faf49fdd0"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (70748-175-30)  / 1 VIAL, SINGLE-DOSE in 1 POUCH / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70748-175-30", "marketing_start_date": "20220727"}, {"sample": false, "description": "60 POUCH in 1 CARTON (70748-175-60)  / 1 VIAL, SINGLE-DOSE in 1 POUCH / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70748-175-60", "marketing_start_date": "20220727"}], "brand_name": "Arformoterol tartrate", "product_id": "70748-175_65d81c00-8791-4937-8e25-4abfc9790e4b", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70748-175", "generic_name": "Arformoterol tartrate", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Arformoterol tartrate", "active_ingredients": [{"name": "ARFORMOTEROL TARTRATE", "strength": "15 ug/2mL"}], "application_number": "ANDA213068", "marketing_category": "ANDA", "marketing_start_date": "20220727", "listing_expiration_date": "20261231"}