All Day Allergy Relief
- Product NDC
- 59726-758
- 11-digit product format
- 597260758
- Labeler code
- 59726
- Product ID
- 59726-758_8478c0ed-6eb2-404b-a86c-5fa12d5b413c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- ANDA075209
- Marketing category
- ANDA
- Marketing start
- 2018-09-30
- Marketing end
- 2024-07-26
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 59726-758-10 | 59726075810 | 10 BLISTER PACK in 1 CARTON (59726-758-10) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2018-09-30 | 0000-00-00 | No | No | Current |