Sunmark
- Product NDC
- 49348-849
- 11-digit product format
- 493480849
- Labeler code
- 49348
- Product ID
- 49348-849_492e6c04-e1a4-41a4-9090-bfe010609c90
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- McKesson
- Application
- ANDA076805
- Marketing category
- ANDA
- Marketing start
- 2004-08-20
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49348-849-34 | Sunmark childrens loratadine | 1 in 1 CARTON | SOLUTION | 1 | | 1 |
| 49348-849-34 | Sunmark childrens loratadine | 120 mL in 1 BOTTLE | SOLUTION | 120 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49348-849 | SUNMARK CHILDRENS LORATADINE (LORATADINE) SOLUTION [MCKESSON] | 1 | Legacy NDC, 2 package rows | 20121114_775731a2-9b30-4a0e-82fb-b517b36317c7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 49348-849-34 | 49348084934 | 1 in 1 CARTON | Historical |