albuterol sulfate

Generic: albuterol sulfate

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name albuterol sulfate
Generic Name albuterol sulfate
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

albuterol sulfate 2 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-671
Product ID 62135-671_fe7cbf82-9f32-327e-e053-6294a90aebc8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA072151
Listing Expiration 2026-12-31
Marketing Start 1989-12-05

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135671
Hyphenated Format 62135-671

Supplemental Identifiers

RxCUI
197316 197318
UPC
0362135672904 0362135671907
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 ANDA072151 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (62135-671-90)
source: ndc

Packages (1)

62135-671-90 90 TABLET in 1 BOTTLE (62135-671-90)

Ingredients (1)

albuterol sulfate (2 mg/1)

Linked Drug Pages (1)

Albuterol Sulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fe7cbf82-9f32-327e-e053-6294a90aebc8", "openfda": {"upc": ["0362135672904", "0362135671907"], "unii": ["021SEF3731"], "rxcui": ["197316", "197318"], "spl_set_id": ["81cdae6f-99d7-468b-9ab8-fecb1d42298d"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-671-90)", "package_ndc": "62135-671-90", "marketing_start_date": "20230614"}], "brand_name": "Albuterol Sulfate", "product_id": "62135-671_fe7cbf82-9f32-327e-e053-6294a90aebc8", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "62135-671", "generic_name": "Albuterol Sulfate", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2 mg/1"}], "application_number": "ANDA072151", "marketing_category": "ANDA", "marketing_start_date": "19891205", "listing_expiration_date": "20261231"}