Levocetirizine Dihydrochloride
- Product NDC
- 60505-3713
- 11-digit product format
- 605053713
- Labeler code
- 60505
- Product ID
- 60505-3713_d10fec00-394e-932f-f237-68b14c9c3505
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levocetirizine Dihydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA203027
- Marketing category
- ANDA
- Marketing start
- 2015-02-13
- Marketing end
- 2021-03-01
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
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 |
|---|
| 60505-3713-9 | 60505371309 | 90 TABLET in 1 BOTTLE (60505-3713-9) | 90 tablet | 2015-02-13 | 2021-03-01 | No | No | Current |