Albuterol Sulfate
- Product NDC
- 67296-1348
- 11-digit product format
- 672961348
- Labeler code
- 67296
- Product ID
- 67296-1348_9c9f7825-f314-4acd-e053-2995a90af8f2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Albuterol Sulfate
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA074454
- Marketing category
- ANDA
- Marketing start
- 2018-01-01
- Marketing end
- 0000-00-00
- Substance
- ALBUTEROL SULFATE
- Active strength
- 2 mg/5mL
- Pharmacologic classes
- Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 67296-1348-1 | Albuterol Sulfate | 120 mL in 1 BOTTLE | SYRUP | 120 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1348 | ALBUTEROL SULFATE SYRUP [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20200121_6ac5a71c-0652-1400-e053-2a91aa0a3e83.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 |
|---|
| 67296-1348-1 | 67296134801 | 120 mL in 1 BOTTLE (67296-1348-1) | 120 ml | 2018-01-01 | 0000-00-00 | No | No | Current |