ALAVERT ALLERGY SINUS D-12
- Product NDC
- 0573-2660
- 11-digit product format
- 005732660
- Labeler code
- 0573
- Product ID
- 0573-2660_60d4d282-c9fb-4d77-b832-80d9d4841eec
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- loratadine, pseudoephedrine sulfate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
- Application
- ANDA076050
- Marketing category
- ANDA
- Marketing start
- 2004-01-30
- Marketing end
- 0000-00-00
- Substance
- LORATADINE; PSEUDOEPHEDRINE SULFATE
- Active strength
- 5 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 0573-2660-12 | 00573266012 | 2 BLISTER PACK in 1 CARTON (0573-2660-12) > 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2004-01-30 | 0000-00-00 | No | No | Current |
| 0573-2660-24 | 00573266024 | 4 BLISTER PACK in 1 CARTON (0573-2660-24) > 6 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | 4 blister pack | 2004-01-30 | 0000-00-00 | No | No | Current |