Albuterol Sulfate
- Product NDC
- 70518-2413
- 11-digit product format
- 705182413
- Labeler code
- 70518
- Product ID
- 70518-2413_dbd4a08a-4199-6aec-e053-2a95a90a0880
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SOLUTION
- Route
- RESPIRATORY (INHALATION)
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074880
- Marketing category
- ANDA
- Marketing start
- 2019-11-11
- 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 |
|---|
| 70518-2413-0 | 70518241300 | 2 POUCH in 1 CARTON (70518-2413-0) > 30 VIAL, SINGLE-DOSE in 1 POUCH > 3 mL in 1 VIAL, SINGLE-DOSE | 2 pouch | 2019-11-11 | 0000-00-00 | No | No | Current |