Loratadine
- Product NDC
- 16714-898
- 11-digit product format
- 167140898
- Labeler code
- 16714
- Product ID
- 16714-898_c892d447-9219-44ac-b9f0-ac3b05ba76eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northstar RxLLC
- Application
- ANDA076301
- Marketing category
- ANDA
- Marketing start
- 2019-02-20
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 16714-898-01 | 16714089801 | 1 BOTTLE in 1 CARTON (16714-898-01) > 30 TABLET in 1 BOTTLE | 1 bottle | 2019-02-20 | 0000-00-00 | No | No | Current |
| 16714-898-02 | 16714089802 | 1 BOTTLE in 1 CARTON (16714-898-02) > 100 TABLET in 1 BOTTLE | 1 bottle | 2019-02-20 | 0000-00-00 | No | No | Current |
| 16714-898-03 | 16714089803 | 1 BOTTLE in 1 CARTON (16714-898-03) > 300 TABLET in 1 BOTTLE | 1 bottle | 2019-02-20 | 0000-00-00 | No | No | Current |