NAUS-EASE
- Product NDC
- 49467-124
- 11-digit product format
- 494670124
- Labeler code
- 49467
- Product ID
- 49467-124_267b73c1-511c-4403-bc3e-45006e02d517
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MECLIZINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Sunascen Therapeutics LLC
- Application
- ANDA040659
- Marketing category
- ANDA
- Marketing start
- 2012-04-16
- Marketing end
- 0000-00-00
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 49467-124-08 | NAUS-EASE | 1 in 1 CARTON | TABLET | 1 | | 7 |
| 49467-124-08 | NAUS-EASE | 8 in 1 BLISTER PACK | TABLET | 8 | | 7 |
| 49467-124-16 | NAUS-EASE | 2 in 1 CARTON | TABLET | 2 | | 7 |
| 49467-124-16 | NAUS-EASE | 8 in 1 BLISTER PACK | TABLET | 8 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49467-124 | NAUS-EASE (MECLIZINE HYDROCHLORIDE) TABLET [SUNASCEN THERAPEUTICS LLC] | 7 | Legacy NDC, 4 package rows | 20230202_43f50d2f-6c27-4b33-b4a8-44e810f93e6f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49467-124-08 | 49467012408 | 1 BLISTER PACK in 1 CARTON (49467-124-08) > 8 TABLET in 1 BLISTER PACK | 1 blister pack | 2012-04-16 | 0000-00-00 | No | No | Current |
| 49467-124-16 | 49467012416 | 2 BLISTER PACK in 1 CARTON (49467-124-16) > 8 TABLET in 1 BLISTER PACK | 2 blister pack | 2012-04-16 | 0000-00-00 | No | No | Current |