Acid Reducer
- Product NDC
- 41250-194
- 11-digit product format
- 412500194
- Labeler code
- 41250
- Product ID
- 41250-194_cface8f8-61ec-402b-b1be-3c8962888688
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- ANDA077351
- Marketing category
- ANDA
- Marketing start
- 2006-09-29
- Marketing end
- 2021-03-31
- Substance
- FAMOTIDINE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 41250-194-02 | 41250019402 | 25 BLISTER PACK in 1 CARTON (41250-194-02) > 1 TABLET in 1 BLISTER PACK | 25 blister pack | 2006-09-29 | 2021-03-31 | No | No | Current |
| 41250-194-71 | 41250019471 | 1 BOTTLE in 1 CARTON (41250-194-71) > 50 TABLET in 1 BOTTLE | 1 bottle | 2006-09-29 | 2021-03-31 | No | No | Current |