Albuterol Sulate
- Product NDC
- 70518-2072
- 11-digit product format
- 705182072
- Labeler code
- 70518
- Product ID
- 70518-2072_499c75ab-2f45-5ba7-e063-6394a90aecfc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- albuterol sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- REMEDYREPACK INC.
- Application
- NDA020983
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-05-13
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Albuterol Sulate
- Brand name suffix
- HFA
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALBUTEROL SULFATE | 90 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 021SEF3731 |
| Rxcui | 2123076 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-2072-0 | Albuterol SulateHFA | 200 in 1 INHALER | AEROSOL, METERED | 200 | | 5 |
| 70518-2072-0 | Albuterol SulateHFA | 1 in 1 CARTON | AEROSOL, METERED | 1 | | 5 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-2072-0 | 70518207200 | 1 INHALER in 1 CARTON (70518-2072-0) / 200 AEROSOL, METERED in 1 INHALER | 1 inhaler | 2019-05-13 | No | No | Current |