Ipratropium Bromide and Albuterol Sulfate
- Product NDC
- 70518-1722
- 11-digit product format
- 705181722
- Labeler code
- 70518
- Product ID
- 70518-1722_963112d9-0d81-7b21-e053-2995a90aa6b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ipratropium bromide and albuterol sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA202496
- Marketing category
- ANDA
- Marketing start
- 2018-12-10
- Marketing end
- 0000-00-00
- Substance
- IPRATROPIUM BROMIDE; ALBUTEROL SULFATE
- Active strength
- 1 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record