sunmark
- Product NDC
- 49348-333
- 11-digit product format
- 493480333
- Labeler code
- 49348
- Product ID
- 49348-333_42c6a214-9cc6-4939-806c-42d8d33cfdcc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- McKesson
- Application
- ANDA076805
- Marketing category
- ANDA
- Marketing start
- 2010-02-27
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 5 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49348-333-34 | sunmark Childrens Loratadine | 120 mL in 1 BOTTLE | SOLUTION | 120 | | 2 |
| 49348-333-34 | sunmark Childrens Loratadine | 1 in 1 CARTON | SOLUTION | 1 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49348-333 | SUNMARK CHILDRENS LORATADINE (LORATADINE) SOLUTION [MCKESSON] | 2 | Legacy NDC, 2 package rows | 20150821_0cd1a8be-4184-4534-99f9-0fcc0dcc5224.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 49348-333-34 | 49348033334 | 120 mL in 1 BOTTLE | 120 ml | Historical |