ALAVERT ALLERGY
- Product NDC
- 0573-2621
- 11-digit product format
- 005732621
- Labeler code
- 0573
- Product ID
- 0573-2621_1ad9e626-55ca-4d43-b5ec-cc4d5bf19b07
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- loratadine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- NDA021375
- Marketing category
- NDA
- Marketing start
- 2002-12-19
- 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 |
|---|
| 0573-2621-13 | 00573262113 | 12 BLISTER PACK in 1 CARTON (0573-2621-13) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 12 blister pack | 2016-12-19 | 0000-00-00 | No | No | Current |
| 0573-2621-19 | 00573262119 | 18 BLISTER PACK in 1 CARTON (0573-2621-19) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 18 blister pack | 2002-12-19 | 0000-00-00 | No | No | Current |
| 0573-2621-65 | 00573262165 | 60 BLISTER PACK in 1 CARTON (0573-2621-65) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 60 blister pack | 2002-12-19 | 0000-00-00 | No | No | Current |