sunmark dual action complete
- Product NDC
- 49348-010
- 11-digit product format
- 493480010
- Labeler code
- 49348
- Product ID
- 49348-010_6c2dc3fc-52b5-40a1-8905-018f8b68144f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- famotidine, calcium carbonate and magnesium hydroxide
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA077355
- Marketing category
- ANDA
- Marketing start
- 2016-01-14
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE; MAGNESIUM HYDROXIDE; CALCIUM CARBONATE
- Active strength
- 10 mg/1; mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record