Loratadine
- Product NDC
- 50268-488
- 11-digit product format
- 502680488
- Labeler code
- 50268
- Product ID
- 50268-488_6d86fdb3-1bd1-2543-e053-2991aa0a884c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA076471
- Marketing category
- ANDA
- Marketing start
- 2016-03-11
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50268-488-11 | EA - Each | 50268-488 | 6d0f5fa6-2445-40eb-b570-2b29e07e9348 | 1 | 2016-04-04 |
| 50268-488-15 | EA - Each | 50268-488 | fcaf1814-aff4-4248-8c95-c80a57382e2b | 1 | 2016-04-04 |