Preferred Plus TabTussin DM
- Product NDC
- 61715-066
- 11-digit product format
- 617150066
- Labeler code
- 61715
- Product ID
- 61715-066_77c7e6a8-cae5-4bfc-a8ee-7c50943235aa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Dextromethorphan Hydrobromide / Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Kinray
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-08-01
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 20 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61715-066 | PREFERRED PLUS TABTUSSIN DM DMTDM (DEXTROMETHORPHAN HYDROBROMIDE / GUAIFENESIN) TABLET [KINRAY] | 1 | Legacy NDC | 20131101_a8cc0249-7933-4747-8780-aa0f09cead7d.zip |