albuterol sulfate

Generic: albuterol sulfate

Labeler: rising pharma holdings, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name albuterol sulfate
Generic Name albuterol sulfate
Labeler rising pharma holdings, inc.
Dosage Form SOLUTION
Routes
RESPIRATORY (INHALATION)
Active Ingredients

albuterol sulfate 2.5 mg/.5mL

Manufacturer
Rising Pharma Holdings, Inc.

Identifiers & Regulatory

Product NDC 64980-642
Product ID 64980-642_33015e7c-a4d2-ecac-e063-6394a90aae00
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075664
Listing Expiration 2026-12-31
Marketing Start 2025-04-14

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 64980642
Hyphenated Format 64980-642

Supplemental Identifiers

RxCUI
245314
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 ANDA075664 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/.5mL
source: ndc
Packaging
  • 30 POUCH in 1 CARTON (64980-642-03) / 1 VIAL, SINGLE-DOSE in 1 POUCH / .5 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

Ingredients (1)

albuterol sulfate (2.5 mg/.5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "33015e7c-a4d2-ecac-e063-6394a90aae00", "openfda": {"unii": ["021SEF3731"], "rxcui": ["245314"], "spl_set_id": ["3236f82c-14e9-dfd4-e063-6294a90ac43d"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (64980-642-03)  / 1 VIAL, SINGLE-DOSE in 1 POUCH / .5 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "64980-642-03", "marketing_start_date": "20250430"}], "brand_name": "Albuterol Sulfate", "product_id": "64980-642_33015e7c-a4d2-ecac-e063-6394a90aae00", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "64980-642", "generic_name": "Albuterol Sulfate", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2.5 mg/.5mL"}], "application_number": "ANDA075664", "marketing_category": "ANDA", "marketing_start_date": "20250414", "listing_expiration_date": "20261231"}