Allergy Relief
- Product NDC
- 69230-312
- 11-digit product format
- 692300312
- Labeler code
- 69230
- Product ID
- 69230-312_7992f72f-e7b7-4e1d-9eb6-ca01603f0f55
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Camber Consumer Care
- Application
- ANDA075209
- Marketing category
- ANDA
- Marketing start
- 2018-12-31
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69230-312-01 | 69230031201 | 1 BOTTLE, PLASTIC in 1 CARTON (69230-312-01) > 100 TABLET in 1 BOTTLE, PLASTIC | | 2018-12-31 | 0000-00-00 | No | No | Current |
| 69230-312-03 | 69230031203 | 300 TABLET in 1 BOTTLE, PLASTIC (69230-312-03) | 300 tablet | 2018-12-31 | 0000-00-00 | No | No | Current |
| 69230-312-30 | 69230031230 | 1 BOTTLE, PLASTIC in 1 BOX (69230-312-30) > 30 TABLET in 1 BOTTLE, PLASTIC | | 2018-12-31 | 0000-00-00 | No | No | Current |