Albuterol sulfate
- Product NDC
- 71205-732
- 11-digit product format
- 712050732
- Labeler code
- 71205
- Product ID
- 71205-732_4ed5342d-7933-406f-93f9-34f45b521ec6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Proficient Rx LP
- Application
- ANDA209954
- Marketing category
- ANDA
- Marketing start
- 2020-08-25
- Substance
- ALBUTEROL SULFATE
- Active strength
- 90 ug/1
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA], beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 021SEF3731 | ALBUTEROL SULFATE | 51022-70-9 | ALBUTEROL SULFATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-732-85 | 71205073285 | 1 CANISTER in 1 CARTON (71205-732-85) / 200 AEROSOL, METERED in 1 CANISTER | 1 canister | 2022-12-21 | No | No | Historical |