acid reducer
- Product NDC
- 11822-0194
- 11-digit product format
- 118220194
- Labeler code
- 11822
- Product ID
- 11822-0194_b032833a-1133-49cf-b798-0995217541eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA077351
- Marketing category
- ANDA
- Marketing start
- 2006-09-29
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0194-3 | 11822019403 | 1 BOTTLE in 1 CARTON (11822-0194-3) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2006-09-29 | 0000-00-00 | No | No | Current |
| 11822-0194-5 | 11822019405 | 25 BLISTER PACK in 1 CARTON (11822-0194-5) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 25 blister pack | 2006-09-29 | 0000-00-00 | No | No | Current |
| 11822-0194-7 | 11822019407 | 2 BOTTLE in 1 CARTON (11822-0194-7) > 85 TABLET, FILM COATED in 1 BOTTLE | 2 bottle | 2006-09-29 | 0000-00-00 | No | No | Current |