Allergy relief
- Product NDC
- 68071-4318
- 11-digit product format
- 680714318
- Labeler code
- 68071
- Product ID
- 68071-4318_bb7a4551-bb3a-7732-e053-2a95a90a6b02
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA076471
- Marketing category
- ANDA
- Marketing start
- 2008-01-01
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 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 |
|---|
| 68071-4318-3 | 68071431803 | 30 TABLET in 1 BOTTLE (68071-4318-3) | 30 tablet | 2018-03-07 | 0000-00-00 | No | No | Current |