levocetirizine dihydrochloride
- Product NDC
- 81086-996
- 11-digit product format
- 810860996
- Labeler code
- 81086
- Product ID
- 81086-996_d3c1633c-03da-8118-e053-2a95a90a5508
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- levocetirizine dihydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Global Distributors, Inc
- Application
- ANDA210375
- Marketing category
- ANDA
- Marketing start
- 2020-12-01
- Marketing end
- 0000-00-00
- Substance
- LEVOCETIRIZINE DIHYDROCHLORIDE
- Active strength
- 5 mg/1
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81086-996-12 | 81086099612 | 1 BOTTLE in 1 CARTON (81086-996-12) > 120 TABLET, COATED in 1 BOTTLE | 1 bottle | 2020-12-01 | 0000-00-00 | No | No | Current |