DRAMAMINE
- Product NDC
- 63029-906
- 11-digit product format
- 630290906
- Labeler code
- 63029
- Product ID
- 63029-906_4c3ea8e1-d98a-45c3-9bce-b85dfe8044a4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MECLIZINE HYDROCHLORIDE
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Medtech Products Inc.
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-02-15
- 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
- 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 | 995632, 2176732 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63029-906-12 | DRAMAMINE | 12 in 1 BLISTER PACK | TABLET, CHEWABLE | 12 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63029-906 | DRAMAMINE (MECLIZINE HYDROCHLORIDE) TABLET, CHEWABLE [MEDTECH PRODUCTS INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20241101_f8cf751a-9f19-4744-a350-cd22303435ee.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63029-906-12 | 63029090612 | 12 TABLET, CHEWABLE in 1 BLISTER PACK (63029-906-12) | 2019-02-15 | 0000-00-00 | No | No | Current |