Sunmark acid reducer
- Product NDC
- 49348-136
- 11-digit product format
- 493480136
- Labeler code
- 49348
- Product ID
- 49348-136_92a95007-47de-4c0c-bc0d-80cd9a07343c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA076195
- Marketing category
- ANDA
- Marketing start
- 2016-05-23
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 49348-136-12 | 49348013612 | 1 BOTTLE in 1 CARTON (49348-136-12) > 60 TABLET, COATED in 1 BOTTLE | 1 bottle | 2016-05-23 | 0000-00-00 | No | No | Current |
| 49348-136-44 | 49348013644 | 1 BOTTLE in 1 CARTON (49348-136-44) > 30 TABLET, COATED in 1 BOTTLE | 1 bottle | 2016-05-23 | 0000-00-00 | No | No | Current |