LORATADINE SOFTGELS
- Product NDC
- 49035-686
- 11-digit product format
- 490350686
- Labeler code
- 49035
- Product ID
- 49035-686_6c50fcac-b085-4473-e053-2a91aa0ae265
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- Wal-Mart Stores Inc
- Application
- ANDA206214
- Marketing category
- ANDA
- Marketing start
- 2018-06-04
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49035-686-30 | LORATADINE SOFTGELS | 30 in 1 BLISTER PACK | CAPSULE, LIQUID FILLED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49035-686 | LORATADINE SOFTGELS (LORATADINE) CAPSULE, LIQUID FILLED [WAL-MART STORES INC] | 1 | Legacy NDC, 1 package rows | 20180604_6c50fcac-b084-4473-e053-2a91aa0ae265.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 49035-686-30 | 49035068630 | 30 in 1 BLISTER PACK | Historical |