ACARBOSE
- Product NDC
- 69543-120
- 11-digit product format
- 695430120
- Labeler code
- 69543
- Product ID
- 69543-120_2fe4e6ff-b000-436f-9a4c-530a190f081f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ACARBOSE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Virtus Pharmaceuticals LLC
- Application
- ANDA091343
- Marketing category
- ANDA
- Marketing start
- 2015-02-01
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69543-120-10 | 69543012010 | 100 TABLET in 1 BOTTLE (69543-120-10) | 100 tablet | 2015-02-01 | 0000-00-00 | No | No | Current |
| 69543-120-11 | 69543012011 | 1000 TABLET in 1 BOTTLE (69543-120-11) | 1000 tablet | 2015-02-01 | 0000-00-00 | No | No | Current |