Mucus D
- Product NDC
- 59779-825
- 11-digit product format
- 597790825
- Labeler code
- 59779
- Product ID
- 59779-825_961ee4f4-3170-4692-9eec-78765a5773d8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin, pseudoephedrine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- CVS Pharmacy
- Application
- ANDA091071
- Marketing category
- ANDA
- Marketing start
- 2015-12-18
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
- Active strength
- 600 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59779-825-68 | 59779082568 | 2 BLISTER PACK in 1 CARTON (59779-825-68) > 18 TABLET in 1 BLISTER PACK | 2 blister pack | 2015-12-18 | 0000-00-00 | No | No | Current |
| 59779-825-89 | 59779082589 | 1 BLISTER PACK in 1 CARTON (59779-825-89) > 18 TABLET in 1 BLISTER PACK | 1 blister pack | 2015-12-18 | 0000-00-00 | No | No | Current |