Acarbose
- Product NDC
- 63629-5697
- 11-digit product format
- 636295697
- Labeler code
- 63629
- Product ID
- 63629-5697_6df81a19-d25e-469a-b2f5-854a809809e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- acarbose
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090912
- Marketing category
- ANDA
- Marketing start
- 2011-07-28
- Marketing end
- 0000-00-00
- Substance
- ACARBOSE
- Active strength
- 25 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 |
|---|
| 63629-5697-1 | Acarbose | 30 in 1 BOTTLE | TABLET | 30 | | 9 |
| 63629-5697-2 | Acarbose | 90 in 1 BOTTLE | TABLET | 90 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-5697 | ACARBOSE TABLET [BRYANT RANCH PREPACK] | 9 | Legacy NDC, 2 package rows | 20231123_1ba7a072-03b0-41f2-be7a-101145bdef3a.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 |
|---|
| 63629-5697-1 | 63629569701 | 30 TABLET in 1 BOTTLE (63629-5697-1) | 30 tablet | 2017-02-07 | 0000-00-00 | No | No | Current |
| 63629-5697-2 | 63629569702 | 90 TABLET in 1 BOTTLE (63629-5697-2) | 90 tablet | 2015-07-17 | 0000-00-00 | No | No | Current |