Mucus Relief Extended Release
- Product NDC
- 55315-732
- 11-digit product format
- 553150732
- Labeler code
- 55315
- Product ID
- 55315-732_ec708689-613e-4e80-bc96-32abea56e6b1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Freds Inc
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2019-02-28
- 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
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 |
|---|
| 55315-732-14 | 55315073214 | 14 BLISTER PACK in 1 CARTON (55315-732-14) > 1 TABLET in 1 BLISTER PACK | 14 blister pack | 2019-02-28 | 0000-00-00 | No | No | Current |