Adult Bisolvine
- Product NDC
- 53145-323
- 11-digit product format
- 531450323
- Labeler code
- 53145
- Product ID
- 53145-323_3d3520bc-498c-922f-e063-6394a90a9a62
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, Dextromethorphan
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- MENPER DISTRIBUTORS INC.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-05-01
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 20; 200 mg/10mL; mg/10mL
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], 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
- Adult Bisolvine
- Brand name suffix
- Adult
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DEXTROMETHORPHAN HYDROBROMIDE | 20 mg/10mL |
| GUAIFENESIN | 200 mg/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9D2RTI9KYH, 495W7451VQ |
| Rxcui | 996520 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53145-323-04 | Adult BisolvineAdult | 120 mL in 1 BOTTLE, PLASTIC | LIQUID | 120 | | 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 |
|---|
| 53145-323-04 | 53145032304 | 120 mL in 1 BOTTLE, PLASTIC (53145-323-04) | 120 ml | 2025-05-01 | No | No | Historical |