Guaifenesin Extended Release 600 mg
- Product NDC
- 62011-0382
- 11-digit product format
- 620110382
- Labeler code
- 62011
- Product ID
- 62011-0382_bd3e14ab-7aa6-4646-a757-17aa99ee71e7
- 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
- 2019-10-17
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62011-0382 | GUAIFENESIN EXTENDED RELEASE 600 MG (GUAIFENESIN) TABLET, EXTENDED RELEASE [STRATEGIC SOURCING SERVICES LLC] | 5 | Legacy NDC | 20220107_d2c4ea2f-dbdc-40e1-96df-a0193560e9ea.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62011-0382-1 | 62011038201 | 4 BLISTER PACK in 1 CARTON (62011-0382-1) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 4 blister pack | 2019-10-17 | 0000-00-00 | No | No | Current |