acid reducer
- Product NDC
- 11822-0141
- 11-digit product format
- 118220141
- Labeler code
- 11822
- Product ID
- 11822-0141_ac9b167c-9705-471d-b127-153879ad3e26
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA075400
- Marketing category
- ANDA
- Marketing start
- 2009-09-10
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 10 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 |
|---|
| 11822-0141-1 | 11822014101 | 2 BOTTLE in 1 CARTON (11822-0141-1) > 90 TABLET, FILM COATED in 1 BOTTLE | 2 bottle | 2009-09-10 | 0000-00-00 | No | No | Current |
| 11822-0141-3 | 11822014103 | 30 BLISTER PACK in 1 CARTON (11822-0141-3) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 30 blister pack | 2009-09-10 | 0000-00-00 | No | No | Current |