Albuterol Sulfate
- Product NDC
- 55154-4350
- 11-digit product format
- 551544350
- Labeler code
- 55154
- Product ID
- 55154-4350_618a93e7-e378-435e-a9fa-0cf3e2d64771
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA075664
- Marketing category
- ANDA
- Marketing start
- 2001-06-26
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 3 mg/.5mL
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55154-4350-5 | 55154435005 | 5 POUCH in 1 BAG (55154-4350-5) > 1 VIAL, SINGLE-DOSE in 1 POUCH > .5 mL in 1 VIAL, SINGLE-DOSE | 5 pouch | 2001-06-26 | 0000-00-00 | No | No | Current |