Guaifenesin Extended-Release Tablets, 600mg
- Product NDC
- 62207-697
- 11-digit product format
- 622070697
- Labeler code
- 62207
- Product ID
- 62207-697_a585f12a-b2f5-f0d2-e053-2a95a90ac1e1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin Extended-Release
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Granules India Ltd
- Application
- ANDA213420
- Marketing category
- ANDA
- Marketing start
- 2020-09-10
- Marketing end
- 0000-00-00
- Substance
- GUAIFENESIN
- Active strength
- 600 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62207-697-72 | 62207069772 | 9 BLISTER PACK in 1 CARTON (62207-697-72) > 10 TABLET in 1 BLISTER PACK | 9 blister pack | 2020-09-10 | 0000-00-00 | No | No | Current |