AKIN DM
- Product NDC
- 69822-201
- 11-digit product format
- 698220201
- Labeler code
- 69822
- Product ID
- 69822-201_3266b146-5198-420d-a0e1-b0809d19747b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DEXTROMETHORPHAN GUAIFENESIN
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Southern Sales & Service, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-01-04
- Marketing end
- 0000-00-00
- Substance
- DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
- Active strength
- 5 mg/5mL; mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69822-201-04 | 69822020104 | 1 BOTTLE in 1 BOX (69822-201-04) > 118 mL in 1 BOTTLE | 1 bottle | 2015-01-01 | 0000-00-00 | No | No | Current |