albuterol

Generic: albuterol

Labeler: zydus lifesciences limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name albuterol
Generic Name albuterol
Labeler zydus lifesciences limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

albuterol sulfate 2 mg/1

Manufacturer
Zydus Lifesciences Limited

Identifiers & Regulatory

Product NDC 70771-1511
Product ID 70771-1511_f4ea29a0-b1df-4ca8-9438-1f0300eb6d9d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208884
Listing Expiration 2026-12-31
Marketing Start 2020-10-23

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 707711511
Hyphenated Format 70771-1511

Supplemental Identifiers

RxCUI
197316 197318
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 (source: ndc)
Generic Name albuterol (source: ndc)
Application Number ANDA208884 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (70771-1511-1)
source: ndc

Packages (1)

70771-1511-1 100 TABLET in 1 BOTTLE (70771-1511-1)

Ingredients (1)

albuterol sulfate (2 mg/1)

Linked Drug Pages (1)

Albuterol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f4ea29a0-b1df-4ca8-9438-1f0300eb6d9d", "openfda": {"unii": ["021SEF3731"], "rxcui": ["197316", "197318"], "spl_set_id": ["a4709eea-e4a2-46e2-850f-1e6afca01893"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1511-1)", "package_ndc": "70771-1511-1", "marketing_start_date": "20201023"}], "brand_name": "Albuterol", "product_id": "70771-1511_f4ea29a0-b1df-4ca8-9438-1f0300eb6d9d", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70771-1511", "generic_name": "Albuterol", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Albuterol", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2 mg/1"}], "application_number": "ANDA208884", "marketing_category": "ANDA", "marketing_start_date": "20201023", "listing_expiration_date": "20261231"}