Albuterol Sulfate
- Product NDC
- 50090-4143
- 11-digit product format
- 500904143
- Labeler code
- 50090
- Product ID
- 50090-4143_e37ff40c-dec1-4c03-838b-4a0b11dffbc6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- albuterol sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- A-S Medication Solutions
- Application
- NDA020983
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-01-15
- Marketing end
- 0000-00-00
- 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
- 2022-12-31
- 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 |
|---|
| 50090-4143-1 | 50090414301 | 1 INHALER in 1 CARTON (50090-4143-1) > 200 AEROSOL, METERED in 1 INHALER | 1 inhaler | 2021-02-24 | 0000-00-00 | No | No | Current |