DRAMAMINE - N
- Product NDC
- 63029-905
- 11-digit product format
- 630290905
- Labeler code
- 63029
- Product ID
- 63029-905_101152a8-cb8e-4f6f-b52a-6667b6343a24
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MECLIZINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Medtech Products Inc.
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-01-15
- Substance
- MECLIZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Antiemetic [EPC], Emesis Suppression [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DRAMAMINE - N
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MECLIZINE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | HDP7W44CIO |
| Rxcui | 995666, 2110527 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63029-905-10 | DRAMAMINE - N | 5 in 1 BLISTER PACK | TABLET | 5 | | 2 |
| 63029-905-10 | DRAMAMINE - N | 2 in 1 BOX | TABLET | 2 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63029-905 | DRAMAMINE - N (MECLIZINE HYDROCHLORIDE) TABLET [MEDTECH PRODUCTS INC.] | 2 | Current NDC, Legacy NDC, 2 package rows | 20241101_7fec7791-c242-4e43-8184-32820e657afb.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 |
|---|
| 63029-905-10 | 63029090510 | 2 BLISTER PACK in 1 BOX (63029-905-10) / 5 TABLET in 1 BLISTER PACK | 2 blister pack | 2018-01-15 | 0000-00-00 | No | No | Current |