Albuterol Sulfate Inhalation Solution
- Product NDC
- 65302-065
- 11-digit product format
- 653020065
- Labeler code
- 65302
- Product ID
- 65302-065_f06d3ff4-0b82-bd33-e053-2a95a90af7e9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- The Ritedose Corporation
- Application
- ANDA214531
- Marketing category
- ANDA
- Marketing start
- 2022-10-07
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 1 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 |
|---|
| 65302-065-05 | 65302006505 | 25 POUCH in 1 CARTON (65302-065-05) > 5 AMPULE in 1 POUCH > 3 mL in 1 AMPULE | 25 pouch | 2022-10-07 | 0000-00-00 | No | No | Current |