non drowsy allergy relief
- Product NDC
- 41250-890
- 11-digit product format
- 412500890
- Labeler code
- 41250
- Product ID
- 41250-890_a567dea7-7d0e-4326-9167-e1e9c4cb8731
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- loratadine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA076011
- Marketing category
- ANDA
- Marketing start
- 2020-09-23
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 7AJO3BO7QN | LORATADINE | 79794-75-5 | LORATADINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 41250-890-65 | 41250089065 | 30 BLISTER PACK in 1 CARTON (41250-890-65) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 30 blister pack | 2020-09-23 | No | No | Historical |