BupropiDex
- Product NDC
- 71598-200
- 11-digit product format
- 715980200
- Labeler code
- 71598
- Product ID
- 71598-200_4081a7ee-5e35-6ad6-e063-6394a90a7047
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DEXTROMETHORPHAN HYDROBROMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DXM Pharmacuetical, Inc.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-12-01
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE
- Active strength
- 15 mg/1
- Pharmacologic classes
- Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- BupropiDex
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEXTROMETHORPHAN HYDROBROMIDE | 15 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9D2RTI9KYH |
| Rxcui | 2173733 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71598-200-15 | BupropiDex | 200 in 1 BOTTLE | TABLET | 200 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71598-200 | BUPROPIDEX (DEXTROMETHORPHAN HYDROBROMIDE) TABLET [DXM PHARMACUETICAL, INC.] | 2 | Current NDC, 1 package rows | 20241009_90cc9bcd-7891-4324-a1f4-f6df7a0457e0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71598-200-15 | 71598020015 | 200 TABLET in 1 BOTTLE (71598-200-15) | 200 tablet | 2023-12-01 | No | No | Historical |