Guaifenesin
- Product NDC
- 30142-703
- 11-digit product format
- 301420703
- Labeler code
- 30142
- Product ID
- 30142-703_9ca44ac2-2482-42ad-a567-18524642a467
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- KROGER COMPANY
- Application
- NDA021282
- Marketing category
- NDA
- Marketing start
- 2017-08-21
- 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
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 |
|---|
| 30142-703-14 | Guaifenesin | 14 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 14 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 30142-703 | GUAIFENESIN TABLET, EXTENDED RELEASE [KROGER COMPANY] | 4 | Legacy NDC, 1 package rows | 20200212_bf2c4ee2-b070-4f07-b53e-79d567cd55be.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30142-703-14 | 30142070314 | 14 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (30142-703-14) | 2017-08-21 | 0000-00-00 | No | No | Current |