heartburn prevention
- Product NDC
- 30142-141
- 11-digit product format
- 301420141
- Labeler code
- 30142
- Product ID
- 30142-141_182928ed-1fa1-4789-901f-c473cf0ea9c0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- ANDA075400
- Marketing category
- ANDA
- Marketing start
- 2009-10-09
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 10 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 table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30142-141-65 | 30142014165 | 30 BLISTER PACK in 1 CARTON (30142-141-65) > 1 TABLET in 1 BLISTER PACK | 30 blister pack | 2009-12-05 | 0000-00-00 | No | No | Current |