Albuterol Sulfate
- Product NDC
- 50090-4138
- 11-digit product format
- 500904138
- Labeler code
- 50090
- Product ID
- 50090-4138_5b5d72ec-27a2-493a-82e1-4097f1b4f0da
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- A-S Medication Solutions
- Application
- NDA021457
- Marketing category
- NDA
- Marketing start
- 2019-01-16
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4138-0 | 50090413800 | 1 INHALER in 1 CARTON (50090-4138-0) > 200 AEROSOL, METERED in 1 INHALER | 1 inhaler | 2019-02-12 | 0000-00-00 | No | No | Current |
| 50090-4138-1 | 50090413801 | 144 INHALER in 1 CASE (50090-4138-1) > 200 AEROSOL, METERED in 1 INHALER | 144 inhaler | 2019-08-21 | 0000-00-00 | No | No | Current |