Mucus Relief Max
- Product NDC
- 21130-206
- 11-digit product format
- 211300206
- Labeler code
- 21130
- Product ID
- 21130-206_a81cba93-0880-496d-b365-870c9eb7ed26
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Safeway
- Application
- ANDA209215
- Marketing category
- ANDA
- Marketing start
- 2018-05-28
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 1200 mg/1
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21130-206-58 | Mucus Relief Max | 2 in 1 CARTON | TABLET, EXTENDED RELEASE | 2 | | 3 |
| 21130-206-58 | Mucus Relief Max | 7 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 7 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-206 | MUCUS RELIEF MAX (GUAIFENESIN) TABLET, EXTENDED RELEASE [SAFEWAY] | 3 | Legacy NDC, 2 package rows | 20221130_947fb8f4-b029-4a75-8bc4-bc6aa6f184fd.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 |
|---|
| 21130-206-58 | 21130020658 | 2 BLISTER PACK in 1 CARTON (21130-206-58) > 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2018-05-28 | 0000-00-00 | No | No | Current |