Loratadine Allergy Relief
- Product NDC
- 53002-7490
- 11-digit product format
- 530027490
- Labeler code
- 53002
- Product ID
- 53002-7490_b1b993b9-119b-4c35-9e35-06bbf360b330
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA076134
- Marketing category
- ANDA
- Marketing start
- 2017-11-01
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 53002-7490-1 | 53002749001 | 10 TABLET in 1 BOTTLE (53002-7490-1) | 10 tablet | 2018-10-01 | 0000-00-00 | No | No | Current |
| 53002-7490-2 | 53002749002 | 20 TABLET in 1 BOTTLE (53002-7490-2) | 20 tablet | 2018-10-01 | 0000-00-00 | No | No | Current |
| 53002-7490-3 | 53002749003 | 30 TABLET in 1 BOTTLE (53002-7490-3) | 30 tablet | 2018-10-01 | 0000-00-00 | No | No | Current |
| 53002-7490-5 | 53002749005 | 15 TABLET in 1 BOTTLE (53002-7490-5) | 15 tablet | 2018-10-01 | 0000-00-00 | No | No | Current |
| 53002-7490-9 | 53002749009 | 5 TABLET in 1 BOTTLE (53002-7490-9) | 5 tablet | 2018-10-01 | 0000-00-00 | No | No | Current |