levocetirizine dihydrochloride
- Product NDC
- 71205-204
- 11-digit product format
- 712050204
- Labeler code
- 71205
- Product ID
- 71205-204_e2a1545c-cbc6-4ea0-a462-17ad0f9a59f0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levocetirizine dihydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA090229
- Marketing category
- ANDA
- Marketing start
- 2010-11-26
- Marketing end
- 0000-00-00
- Substance
- LEVOCETIRIZINE DIHYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 71205-204 | LEVOCETIRIZINE DIHYDROCHLORIDE TABLET [PROFICIENT RX LP] | 2 | Legacy NDC | 20191012_93d3a3bd-cfaa-422b-86aa-cc664ec58530.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-204-30 | 71205020430 | 30 TABLET in 1 BOTTLE (71205-204-30) | 30 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |
| 71205-204-60 | 71205020460 | 60 TABLET in 1 BOTTLE (71205-204-60) | 60 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |
| 71205-204-90 | 71205020490 | 90 TABLET in 1 BOTTLE (71205-204-90) | 90 tablet | 2019-01-01 | 0000-00-00 | No | No | Current |