sunmark mucus er
- Product NDC
- 70677-0035
- 11-digit product format
- 706770035
- Labeler code
- 70677
- Product ID
- 70677-0035_141b786e-6067-481e-b714-90ece4278249
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA091009
- Marketing category
- ANDA
- Marketing start
- 2017-09-07
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 1200 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 70677-0035-1 | 70677003501 | 1 BOTTLE in 1 CARTON (70677-0035-1) > 14 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2017-09-07 | 0000-00-00 | No | No | Current |