Guaifenesin
- Product NDC
- 69842-016
- 11-digit product format
- 698420016
- Labeler code
- 69842
- Product ID
- 69842-016_b4ea3a57-e79c-40a2-83cc-01e40a7eac82
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- CVS PHARMACY
- 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
- 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 |
|---|
| 69842-016-14 | GuaifenesinExtended Release | 1 in 1 CARTON | TABLET, EXTENDED RELEASE | 1 | | 3 |
| 69842-016-14 | GuaifenesinExtended Release | 14 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 14 | | 3 |
| 69842-016-28 | GuaifenesinExtended Release | 14 in 1 BLISTER PACK | TABLET, EXTENDED RELEASE | 14 | | 3 |
| 69842-016-28 | GuaifenesinExtended Release | 2 in 1 CARTON | TABLET, EXTENDED RELEASE | 2 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69842-016 | GUAIFENESIN EXTENDED RELEASE (GUAIFENESIN) TABLET, EXTENDED RELEASE [CVS PHARMACY] | 3 | Legacy NDC, 4 package rows | 20181213_2c75f0cf-158d-4f68-955b-c2fc11192789.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 69842-016-14 | 69842001614 | 1 in 1 CARTON | Historical |
| 69842-016-28 | 69842001628 | 14 in 1 BLISTER PACK | Historical |