AMBRISENTAN
- Product NDC
- 42291-019
- 11-digit product format
- 422910019
- Labeler code
- 42291
- Product ID
- 42291-019_b6c019e2-3f31-061d-e053-2a95a90a89d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMBRISENTAN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA208354
- Marketing category
- ANDA
- Marketing start
- 2020-12-18
- Marketing end
- 0000-00-00
- Substance
- AMBRISENTAN
- Active strength
- 10 mg/1
- Pharmacologic classes
- Endothelin Receptor Antagonist [EPC],Endothelin Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-019-30 | 42291001930 | 30 TABLET, FILM COATED in 1 BOTTLE (42291-019-30) | 2020-12-18 | 0000-00-00 | No | No | Current |