Sunmark acid reducer
- Product NDC
- 49348-109
- 11-digit product format
- 493480109
- Labeler code
- 49348
- Product ID
- 49348-109_8e94dbdd-8634-49fd-b7d6-2fa337f8b1cd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA091429
- Marketing category
- ANDA
- Marketing start
- 2016-06-14
- Marketing end
- 2021-07-31
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 49348-109-04 | 49348010904 | 1 BOTTLE in 1 CARTON (49348-109-04) > 24 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2016-06-14 | 0000-00-00 | No | No | Current |
| 49348-109-54 | 49348010954 | 1 BOTTLE in 1 CARTON (49348-109-54) > 65 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2016-06-14 | 0000-00-00 | No | No | Current |