Dimenhydrinate
- Product NDC
- 0904-6772
- 11-digit product format
- 009046772
- Labeler code
- 0904
- Product ID
- 0904-6772_3c44729b-0a55-8eaf-e063-6394a90a5ba4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dimenhydrinate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- M009
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-02-14
- Marketing end
- 2028-08-31
- Substance
- DIMENHYDRINATE
- Active strength
- 50 mg/1
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dimenhydrinate
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIMENHYDRINATE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | JB937PER5C |
| Rxcui | 198603 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-6772-12 | Dimenhydrinate | 12 in 1 BLISTER PACK | TABLET | 12 | | 4 |
| 0904-6772-12 | Dimenhydrinate | 1 in 1 CARTON | TABLET | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-6772 | DIMENHYDRINATE TABLET [MAJOR PHARMACEUTICALS] | 3 | Current NDC, Legacy NDC, 2 package rows | 20240507_78d22836-a442-7c0c-e053-2991aa0a62f3.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 |
|---|
| 0904-6772-12 | 00904677212 | 1 BLISTER PACK in 1 CARTON (0904-6772-12) / 12 TABLET in 1 BLISTER PACK | 1 blister pack | 2019-02-14 | 2028-08-31 | No | No | Current |