DRAMAMINE
- Product NDC
- 63029-913
- 11-digit product format
- 630290913
- Labeler code
- 63029
- Product ID
- 63029-913_5484a85b-4c87-41a4-bf00-3d96933f4eb9
- 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
- 2026-02-02
- 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 |
|---|
| 63029-913-12 | DRAMAMINE | 1 in 1 BOX | TABLET, CHEWABLE | 1 | | 1 |
| 63029-913-12 | DRAMAMINE | 12 in 1 BLISTER PACK | TABLET, CHEWABLE | 12 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 63029-913-12 | 63029091312 | 1 BLISTER PACK in 1 BOX (63029-913-12) / 12 TABLET, CHEWABLE in 1 BLISTER PACK | 1 blister pack | 2026-02-02 | No | No | Historical |