Albuterol Sulfate
- Product NDC
- 68071-2367
- 11-digit product format
- 680712367
- Labeler code
- 68071
- Product ID
- 68071-2367_bdad8ca9-0130-1991-e053-2995a90ae695
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- NDA020503
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-04-03
- Marketing end
- 2022-12-31
- Substance
- ALBUTEROL SULFATE
- Active strength
- 108 ug/1
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-2367-6 | 68071236706 | 1 CANISTER in 1 CARTON (68071-2367-6) > 200 AEROSOL, METERED in 1 CANISTER | 1 canister | 2019-04-03 | 2022-12-31 | No | No | Current |