ipratropium bromide and albuterol sulfate

Generic: ipratropium bromide and albuterol sulfate

Labeler: cipla usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ipratropium bromide and albuterol sulfate
Generic Name ipratropium bromide and albuterol sulfate
Labeler cipla usa inc.
Dosage Form SOLUTION
Routes
RESPIRATORY (INHALATION)
Active Ingredients

albuterol sulfate 2.5 mg/3mL, ipratropium bromide .5 mg/3mL

Manufacturer
Cipla USA Inc.

Identifiers & Regulatory

Product NDC 69097-840
Product ID 69097-840_14b7dfcc-b3a8-4027-9544-8d52ec2aacf3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202496
Listing Expiration 2026-12-31
Marketing Start 2020-06-01

Pharmacologic Class

Classes
adrenergic beta2-agonists [moa] anticholinergic [epc] cholinergic antagonists [moa] beta2-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69097840
Hyphenated Format 69097-840

Supplemental Identifiers

RxCUI
1437702
UNII
021SEF3731 J697UZ2A9J

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 ipratropium bromide and albuterol sulfate (source: ndc)
Generic Name ipratropium bromide and albuterol sulfate (source: ndc)
Application Number ANDA202496 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 2.5 mg/3mL
  • .5 mg/3mL
source: ndc
Packaging
  • 30 POUCH in 1 CARTON (69097-840-53) / 1 VIAL in 1 POUCH (69097-840-34) / 3 mL in 1 VIAL
  • 2 POUCH in 1 CARTON (69097-840-64) / 30 VIAL in 1 POUCH / 3 mL in 1 VIAL
  • 1 POUCH in 1 CARTON (69097-840-87) / 30 VIAL in 1 POUCH / 3 mL in 1 VIAL
source: ndc

Packages (3)

Ingredients (2)

albuterol sulfate (2.5 mg/3mL) ipratropium bromide (.5 mg/3mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "14b7dfcc-b3a8-4027-9544-8d52ec2aacf3", "openfda": {"unii": ["021SEF3731", "J697UZ2A9J"], "rxcui": ["1437702"], "spl_set_id": ["89d59bd9-c826-413c-8ed9-a1521a0c7cc5"], "manufacturer_name": ["Cipla USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (69097-840-53)  / 1 VIAL in 1 POUCH (69097-840-34)  / 3 mL in 1 VIAL", "package_ndc": "69097-840-53", "marketing_start_date": "20200601"}, {"sample": false, "description": "2 POUCH in 1 CARTON (69097-840-64)  / 30 VIAL in 1 POUCH / 3 mL in 1 VIAL", "package_ndc": "69097-840-64", "marketing_start_date": "20200601"}, {"sample": false, "description": "1 POUCH in 1 CARTON (69097-840-87)  / 30 VIAL in 1 POUCH / 3 mL in 1 VIAL", "package_ndc": "69097-840-87", "marketing_start_date": "20200601"}], "brand_name": "Ipratropium Bromide and Albuterol Sulfate", "product_id": "69097-840_14b7dfcc-b3a8-4027-9544-8d52ec2aacf3", "dosage_form": "SOLUTION", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "69097-840", "generic_name": "Ipratropium Bromide and Albuterol Sulfate", "labeler_name": "Cipla USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ipratropium Bromide and Albuterol Sulfate", "active_ingredients": [{"name": "ALBUTEROL SULFATE", "strength": "2.5 mg/3mL"}, {"name": "IPRATROPIUM BROMIDE", "strength": ".5 mg/3mL"}], "application_number": "ANDA202496", "marketing_category": "ANDA", "marketing_start_date": "20200601", "listing_expiration_date": "20261231"}