Mucus Relief
- Product NDC
- 69230-314
- 11-digit product format
- 692300314
- Labeler code
- 69230
- Product ID
- 69230-314_4d7d2858-634b-44a0-888b-9ad75ae29845
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Camber Consumer Care
- Application
- ANDA209215
- Marketing category
- ANDA
- Marketing start
- 2019-11-06
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69230-314-31 | 69230031431 | 1 BLISTER PACK in 1 CARTON (69230-314-31) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 1 blister pack | 2019-11-06 | 0000-00-00 | No | No | Current |
| 69230-314-32 | 69230031432 | 2 BLISTER PACK in 1 CARTON (69230-314-32) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 2 blister pack | 2019-11-06 | 0000-00-00 | No | No | Current |