Loratadine
- Product NDC
- 70985-017
- 11-digit product format
- 709850017
- Labeler code
- 70985
- Product ID
- 70985-017_c5c02d48-4206-483d-e053-2995a90a56c1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DRUG OCEAN LLC
- Application
- ANDA214684
- Marketing category
- ANDA
- Marketing start
- 2021-06-27
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70985-017 | LORATADINE TABLET [DRUG OCEAN LLC] | 3 | Legacy NDC | 20231023_bd6cd66b-1144-4d0b-b13a-230590b398e4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70985-017-01 | 70985001701 | 100 TABLET in 1 PACKAGE (70985-017-01) | 100 tablet | 2021-06-27 | 0000-00-00 | No | No | Current |
| 70985-017-10 | 70985001710 | 10 TABLET in 1 BLISTER PACK (70985-017-10) | 10 tablet | 2021-06-27 | 0000-00-00 | No | No | Current |