Mucus Relief Extended Release
- Product NDC
- 41250-732
- 11-digit product format
- 412500732
- Labeler code
- 41250
- Product ID
- 41250-732_1bbce63b-1222-46ed-b0b5-7eb3f82471ae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- MEIJER, INC.
- Application
- ANDA207342
- Marketing category
- ANDA
- Marketing start
- 2018-07-11
- 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
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41250-732-14 | 41250073214 | 14 BLISTER PACK in 1 CARTON (41250-732-14) > 1 TABLET in 1 BLISTER PACK | 14 blister pack | 2018-07-11 | 0000-00-00 | No | No | Current |
| 41250-732-42 | 41250073242 | 42 BLISTER PACK in 1 CARTON (41250-732-42) > 1 TABLET in 1 BLISTER PACK | 42 blister pack | 2018-07-11 | 0000-00-00 | No | No | Current |