sunmark acid reducer
- Product NDC
- 49348-128
- 11-digit product format
- 493480128
- Labeler code
- 49348
- Product ID
- 49348-128_646e3d4d-6e53-44fc-a343-6294c0d97aa0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- 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 |
|---|
| 49348-128-12 | 49348012812 | 1 BOTTLE in 1 CARTON (49348-128-12) > 60 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2009-09-10 | 0000-00-00 | No | No | Current |
| 49348-128-13 | 49348012813 | 1 BOTTLE in 1 CARTON (49348-128-13) > 90 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2009-11-04 | 0000-00-00 | No | No | Current |
| 49348-128-44 | 49348012844 | 30 BLISTER PACK in 1 CARTON (49348-128-44) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 30 blister pack | 2009-10-14 | 0000-00-00 | No | No | Current |