Albuterol Sulfate
- Product NDC
- 55154-4359
- 11-digit product format
- 551544359
- Labeler code
- 55154
- Product ID
- 55154-4359_34dc1e08-85b8-4772-a7ef-3f5d880bd594
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA074880
- Marketing category
- ANDA
- Marketing start
- 1997-09-17
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 3 mg/3mL
- 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 |
|---|
| 55154-4359-5 | 55154435905 | 5 POUCH in 1 BAG (55154-4359-5) > 1 VIAL, SINGLE-DOSE in 1 POUCH > 3 mL in 1 VIAL, SINGLE-DOSE | 5 pouch | 1997-09-17 | 0000-00-00 | No | No | Current |