albuterol sulfate
- Product NDC
- 71205-441
- 11-digit product format
- 712050441
- Labeler code
- 71205
- Product ID
- 71205-441_539823ee-064c-4094-a74c-b50a07a80bf2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- albuterol sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- Proficient Rx LP
- Application
- ANDA203760
- Marketing category
- ANDA
- Marketing start
- 2020-02-26
- 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 |
|---|
| 71205-441-85 | 71205044185 | 1 INHALER in 1 CARTON (71205-441-85) / 200 AEROSOL, METERED in 1 INHALER | 1 inhaler | 2020-04-01 | No | No | Historical |