allergy congestion relief
- Product NDC
- 30142-846
- 11-digit product format
- 301420846
- Labeler code
- 30142
- Product ID
- 30142-846_31a983e6-c7eb-4a48-8ada-c0cbac319c74
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- loratadine, pseudoephedrine sulfate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA075989
- Marketing category
- ANDA
- Marketing start
- 2024-02-22
- Substance
- LORATADINE; PSEUDOEPHEDRINE SULFATE
- Active strength
- 10; 240 mg/1; mg/1
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
- 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 |
| Y9DL7QPE6B | PSEUDOEPHEDRINE SULFATE | 7460-12-0 | PSEUDOEPHEDRINE SULFATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 30142-846-22 | 30142084622 | 15 BLISTER PACK in 1 CARTON (30142-846-22) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 15 blister pack | 2024-02-22 | No | No | Historical |