7 Select Acid Controller
- Product NDC
- 10202-194
- 11-digit product format
- 102020194
- Labeler code
- 10202
- Product ID
- 10202-194_7651452d-e7a4-46d1-ab8e-091113d42b94
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- 7-Eleven
- Application
- ANDA077351
- Marketing category
- ANDA
- Marketing start
- 2014-08-05
- Marketing end
- 2020-01-31
- Substance
- FAMOTIDINE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record