ACARBOSE
- Product NDC
- 50090-5088
- 11-digit product format
- 500905088
- Labeler code
- 50090
- Product ID
- 50090-5088_c61e545d-f38c-4dce-905c-ef3f04d21c6c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ACARBOSE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091343
- Marketing category
- ANDA
- Marketing start
- 2015-02-01
- Marketing end
- 0000-00-00
- Substance
- ACARBOSE
- Active strength
- 100 mg/1
- Pharmacologic classes
- alpha Glucosidase Inhibitors [MoA],alpha-Glucosidase Inhibitor [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 |
|---|
| 50090-5088-0 | ACARBOSE | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5088 | ACARBOSE TABLET [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 1 package rows | 20200701_1d5412c5-8dfa-4f9e-bad9-8162d84ae957.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 |
|---|
| 50090-5088-0 | 50090508800 | 30 TABLET in 1 BOTTLE (50090-5088-0) | 30 tablet | 2020-06-29 | 0000-00-00 | No | No | Current |