Claritin
- Product NDC
- 85237-1630
- 11-digit product format
- 852371630
- Labeler code
- 85237
- Product ID
- 85237-1630_46fe1007-0c18-a3ba-e063-6394a90a7b11
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Select Consumer Group
- Application
- ANDA075209
- Marketing category
- ANDA
- Marketing start
- 2020-12-01
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Claritin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LORATADINE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7AJO3BO7QN |
| Rxcui | 206805, 311372 |
DailyMed Package Descriptions#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85237-1630-1 | 85237163001 | 1 BLISTER PACK in 1 CARTON (85237-1630-1) / 1 TABLET in 1 BLISTER PACK | 1 blister pack | 2025-08-18 | No | No | Current |
| 85237-1630-3 | 85237163003 | 20 POUCH in 1 BOX, UNIT-DOSE (85237-1630-3) / 1 TABLET in 1 POUCH | 20 pouch | 2025-12-27 | No | No | Current |
| 85237-1630-4 | 85237163004 | 25 POUCH in 1 BOX, UNIT-DOSE (85237-1630-4) / 1 TABLET in 1 POUCH | 25 pouch | 2025-12-27 | No | No | Current |