Broncomar
- Product NDC
- 70242-101
- 11-digit product format
- 702420101
- Labeler code
- 70242
- Product ID
- 70242-101_b0882739-0e4e-4942-a99f-916a34ee24ba
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan HBr, Guaifenesin
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Dannso Corp./d.b.a. Essential Products
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2001-10-01
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 10 mg/5mL; mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70242-101-06 | BroncomarDM | 177 mL in 1 BOTTLE | LIQUID | 177 | | 2 |
| 70242-101-06 | BroncomarDM | 1 in 1 CARTON | LIQUID | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70242-101 | BRONCOMAR DM (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [DANNSO CORP./D.B.A. ESSENTIAL PRODUCTS] | 2 | Legacy NDC, 2 package rows | 20200925_6d33888d-cbde-4f67-ade7-60cdbfcb2169.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 |
|---|
| 70242-101-06 | 70242010106 | 1 BOTTLE in 1 CARTON (70242-101-06) > 177 mL in 1 BOTTLE | 1 bottle | 2015-01-01 | 0000-00-00 | No | No | Current |