albuterol sulfate

Generic: albuterol sulfate

Labeler: quagen pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name albuterol sulfate
Generic Name albuterol sulfate
Labeler quagen pharmaceuticals llc
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

albuterol sulfate 2 mg/5mL

Manufacturer
QUAGEN PHARMACEUTICALS LLC

Identifiers & Regulatory

Product NDC 70752-102
Product ID 70752-102_f8b35fdc-741f-4ebd-91d5-a55a7ef8e261
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212197
Listing Expiration 2026-12-31
Marketing Start 2019-09-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70752102
Hyphenated Format 70752-102

Supplemental Identifiers

RxCUI
755497
UPC
0370752102124
UNII
021SEF3731

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 albuterol sulfate (source: ndc)
Generic Name albuterol sulfate (source: ndc)
Application Number ANDA212197 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/5mL
source: ndc
Packaging
  • 473 mL in 1 BOTTLE (70752-102-12)
source: ndc

Packages (1)

70752-102-12 473 mL in 1 BOTTLE (70752-102-12)

Ingredients (1)

albuterol sulfate (2 mg/5mL)

Linked Drug Pages (1)

ALBUTEROL SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f8b35fdc-741f-4ebd-91d5-a55a7ef8e261", "openfda": {"upc": ["0370752102124"], "unii": ["021SEF3731"], "rxcui": ["755497"], "spl_set_id": ["99a490cc-e41d-436b-9cf3-8facb7ac714f"], "manufacturer_name": ["QUAGEN PHARMACEUTICALS LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (70752-102-12)", "package_ndc": "70752-102-12", "marketing_start_date": "20190906"}], "brand_name": "ALBUTEROL SULFATE", "product_id": "70752-102_f8b35fdc-741f-4ebd-91d5-a55a7ef8e261", "dosage_form": "SYRUP", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70752-102", "generic_name": "ALBUTEROL SULFATE", "labeler_name": "QUAGEN PHARMACEUTICALS LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ALBUTEROL SULFATE", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2 mg/5mL"}], "application_number": "ANDA212197", "marketing_category": "ANDA", "marketing_start_date": "20190906", "listing_expiration_date": "20261231"}