albuterol sulfate
- Product NDC
- 51407-367
- 11-digit product format
- 514070367
- Labeler code
- 51407
- Product ID
- 51407-367_4f875ac2-2a69-dbc3-e063-6394a90a31f1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- albuterol sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA072637
- Marketing category
- ANDA
- Marketing start
- 1989-12-05
- Substance
- ALBUTEROL SULFATE
- Active strength
- 2 mg/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 sulfate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALBUTEROL SULFATE | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 021SEF3731 |
| Rxcui | 197316, 197318 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51407-367-01 | albuterol sulfate | 100 in 1 BOTTLE | TABLET | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51407-367 | ALBUTEROL SULFATE TABLET [GOLDEN STATE MEDICAL SUPPLY] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231020_a22af54a-c010-ab8b-e053-2a95a90a8862.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-367-01 | 51407036701 | 100 TABLET in 1 BOTTLE (51407-367-01) | 100 tablet | 2020-03-26 | 0000-00-00 | No | No | Current |