LEVOCETIRIZINE DIHYDROCHLORIDE
- Product NDC
- 70518-2146
- 11-digit product format
- 705182146
- Labeler code
- 70518
- Product ID
- 70518-2146_c69d4156-ed7b-b8ac-e053-2995a90a6c8b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVOCETIRIZINE DIHYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205564
- Marketing category
- ANDA
- Marketing start
- 2019-06-12
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2146-0 | 70518214600 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2146-0) | 2019-06-12 | 0000-00-00 | No | No | Current |