Loratadine Allergy Relief
- Product NDC
- 55700-097
- 11-digit product format
- 557000097
- Labeler code
- 55700
- Product ID
- 55700-097_8b07bc13-cd2a-49a6-b16b-cbfe1360bdcf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA076134
- Marketing category
- ANDA
- Marketing start
- 2003-08-28
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- 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 |
|---|
| 55700-097-30 | 55700009730 | 30 TABLET in 1 BOTTLE (55700-097-30) | 30 tablet | 2014-01-31 | 0000-00-00 | No | No | Current |
| 55700-097-90 | 55700009790 | 90 TABLET in 1 BOTTLE (55700-097-90) | 90 tablet | 2014-01-31 | 0000-00-00 | No | No | Current |