Ipratropium Bromide and Albuterol Sulfate
- Product NDC
- 65302-047
- 11-digit product format
- 653020047
- Labeler code
- 65302
- Product ID
- 65302-047_9d49f1ff-409c-7eb8-e053-2a95a90a29b4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ipratropium Bromide and Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- The Ritedose Corporation
- Application
- ANDA202496
- Marketing category
- ANDA
- Marketing start
- 2018-12-15
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE; IPRATROPIUM BROMIDE
- Active strength
- 3 mg/3mL; mg/3mL
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA],Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record