Loratadine
- Product NDC
- 70677-0134
- 11-digit product format
- 706770134
- Labeler code
- 70677
- Product ID
- 70677-0134_ef3fd1e7-6f4d-7bbe-e053-2a95a90ab95d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Strategic Sourcing Services, LLC
- Application
- ANDA214684
- Marketing category
- ANDA
- Marketing start
- 2021-07-06
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70677-0134-1 | 70677013401 | 30 TABLET in 1 BOTTLE (70677-0134-1) | 30 tablet | 2021-07-06 | 0000-00-00 | No | No | Current |