Albuterol Sulate
- Product NDC
- 68071-4777
- 11-digit product format
- 680714777
- Labeler code
- 68071
- Product ID
- 68071-4777_3dd46e51-9131-c009-e063-6394a90ae5a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- albuterol sulfate
- Dosage form
- AEROSOL, METERED
- Route
- RESPIRATORY (INHALATION)
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- NDA020983
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-01-15
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Albuterol Sulate
- Brand name suffix
- HFA
- Listing expiration
- 2026-12-31
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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-4777-2 | Albuterol SulateHFA | 200 in 1 INHALER | AEROSOL, METERED | 200 | | 6 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4777-2 | 68071477702 | 200 AEROSOL, METERED in 1 INHALER (68071-4777-2) | 2019-02-20 | 0000-00-00 | No | No | Current |