levocetirizine dihydrochloride
- Product NDC
- 70518-3366
- 11-digit product format
- 705183366
- Labeler code
- 70518
- Product ID
- 70518-3366_d812bcaf-1939-58b1-e053-2995a90ab86c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levocetirizine dihydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA203646
- Marketing category
- ANDA
- Marketing start
- 2022-02-14
- 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
- 2023-12-31
- 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 |
|---|
| 70518-3366-0 | 70518336600 | 30 TABLET in 1 BOTTLE, PLASTIC (70518-3366-0) | 30 tablet | 2022-02-14 | 0000-00-00 | No | No | Current |