Irbesartan
- Product NDC
- 71205-404
- 11-digit product format
- 712050404
- Labeler code
- 71205
- Product ID
- 71205-404_26b07048-78ca-46f4-bc10-b78fe387321a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- irbesartan
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA020757
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-09-03
- Marketing end
- 0000-00-00
- Substance
- IRBESARTAN
- Active strength
- 75 mg/1
- Pharmacologic classes
- Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-404 | IRBESARTAN TABLET, FILM COATED [PROFICIENT RX LP] | 2 | Legacy NDC | 20200702_909f7937-3790-4aa4-addd-166040193eca.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-404-30 | 71205040430 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-404-30) | 2020-02-17 | 0000-00-00 | No | No | Current |
| 71205-404-60 | 71205040460 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-404-60) | 2020-02-17 | 0000-00-00 | No | No | Current |
| 71205-404-90 | 71205040490 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-404-90) | 2020-02-17 | 0000-00-00 | No | No | Current |