Mucus
- Product NDC
- 63868-389
- 11-digit product format
- 638680389
- Labeler code
- 63868
- Product ID
- 63868-389_f6425f37-7a3a-44d8-8173-84a8f4bc0c29
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- CHAIN DRUG MARKETING ASSOCIATION INC
- Application
- NDA021282
- Marketing category
- NDA
- Marketing start
- 2018-02-08
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63868-389-20 | Mucus | 20 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 20 | | 5 |
| 63868-389-20 | Mucus | 1 in 1 CARTON | TABLET, EXTENDED RELEASE | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63868-389 | MUCUS (GUAIFENESIN) TABLET, EXTENDED RELEASE [CHAIN DRUG MARKETING ASSOCIATION INC] | 5 | Legacy NDC, 2 package rows | 20190109_b6b1fe99-4b03-4b1c-8b0c-66ba5cb129f2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 63868-389-20 | 63868038920 | 20 in 1 BLISTER PACK | Historical |