Sunmark Mucus Relief
- Product NDC
- 70677-0055
- 11-digit product format
- 706770055
- Labeler code
- 70677
- Product ID
- 70677-0055_aa6a0923-2316-476f-9b8a-69ed302a1bd1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA209215
- Marketing category
- ANDA
- Marketing start
- 2018-07-22
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70677-0055-1 | Sunmark Mucus Relief | 10 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 10 | | 5 |
| 70677-0055-1 | Sunmark Mucus Relief | 4 in 1 CARTON | TABLET, EXTENDED RELEASE | 4 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70677-0055 | SUNMARK MUCUS RELIEF (GUAIFENESIN) TABLET, EXTENDED RELEASE [STRATEGIC SOURCING SERVICES LLC] | 5 | Legacy NDC, 2 package rows | 20241215_41a3adc9-22ca-4409-ba07-3f6ea3b68cf2.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 |
|---|
| 70677-0055-1 | 70677005501 | 4 BLISTER PACK in 1 CARTON (70677-0055-1) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 4 blister pack | 2019-09-26 | 0000-00-00 | No | No | Current |