Sunmark Loratadine
- Product NDC
- 49348-818
- 11-digit product format
- 493480818
- Labeler code
- 49348
- Product ID
- 49348-818_b14990f8-9e84-4d8a-8e28-a9f2271254f7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA076301
- Marketing category
- ANDA
- Marketing start
- 2007-06-21
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 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 |
|---|
| 49348-818-01 | 49348081801 | 10 BLISTER PACK in 1 CARTON (49348-818-01) > 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2007-06-25 | 0000-00-00 | No | No | Current |
| 49348-818-13 | 49348081813 | 1 BOTTLE in 1 CARTON (49348-818-13) > 90 TABLET in 1 BOTTLE | 1 bottle | 2007-06-21 | 0000-00-00 | No | No | Current |
| 49348-818-44 | 49348081844 | 30 BLISTER PACK in 1 CARTON (49348-818-44) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2007-06-21 | 0000-00-00 | No | No | Current |
| 49348-818-45 | 49348081845 | 1 BOTTLE in 1 CARTON (49348-818-45) > 30 TABLET in 1 BOTTLE | 1 bottle | 2018-10-24 | 0000-00-00 | No | No | Current |
| 49348-818-56 | 49348081856 | 1 BOTTLE in 1 CARTON (49348-818-56) > 70 TABLET in 1 BOTTLE | 1 bottle | 2014-03-31 | 0000-00-00 | No | No | Current |