maximum strength mucus relief
- Product NDC
- 41250-672
- 11-digit product format
- 412500672
- Labeler code
- 41250
- Product ID
- 41250-672_b0b9f25e-b7a2-4ae4-843f-621af2a94ff4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA091009
- Marketing category
- ANDA
- Marketing start
- 2020-09-23
- 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
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41250-672-55 | 41250067255 | 1 BOTTLE in 1 CARTON (41250-672-55) > 42 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2020-09-23 | 0000-00-00 | No | No | Current |
| 41250-672-66 | 41250067266 | 1 BOTTLE in 1 CARTON (41250-672-66) > 14 TABLET, EXTENDED RELEASE in 1 BOTTLE | 1 bottle | 2020-09-23 | 0000-00-00 | No | No | Current |