albuterol sulfate
Generic: albuterol sulfate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
albuterol sulfate
Generic Name
albuterol sulfate
Labeler
remedyrepack inc.
Dosage Form
AEROSOL, METERED
Routes
Active Ingredients
albuterol sulfate 108 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4528
Product ID
70518-4528_450d43d4-5770-2263-e063-6294a90a583d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA020503
Listing Expiration
2026-12-31
Marketing Start
2025-12-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184528
Hyphenated Format
70518-4528
Supplemental Identifiers
RxCUI
UNII
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
NDA020503 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 108 ug/1
Packaging
- 1 CANISTER in 1 CARTON (70518-4528-0) / 200 AEROSOL, METERED in 1 CANISTER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "450d43d4-5770-2263-e063-6294a90a583d", "openfda": {"unii": ["021SEF3731"], "rxcui": ["2123111"], "spl_set_id": ["32dbec5e-044a-40b6-9b88-e1396c4b4b6e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 CANISTER in 1 CARTON (70518-4528-0) / 200 AEROSOL, METERED in 1 CANISTER", "package_ndc": "70518-4528-0", "marketing_start_date": "20251203"}], "brand_name": "Albuterol Sulfate", "product_id": "70518-4528_450d43d4-5770-2263-e063-6294a90a583d", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-4528", "generic_name": "Albuterol Sulfate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "108 ug/1"}], "application_number": "NDA020503", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20251203", "listing_expiration_date": "20261231"}