sunmark lansoprazole
- Product NDC
- 49348-301
- 11-digit product format
- 493480301
- Labeler code
- 49348
- Product ID
- 49348-301_0257b87a-67c6-45ac-98c5-743ff20d1520
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Strategic Sourcing Services LLC
- Application
- ANDA202319
- Marketing category
- ANDA
- Marketing start
- 2012-05-21
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 49348-301-46 | 49348030146 | 1 BOTTLE in 1 CARTON (49348-301-46) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2012-05-21 | 0000-00-00 | No | No | Current |
| 49348-301-61 | 49348030161 | 3 BOTTLE in 1 CARTON (49348-301-61) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2012-05-21 | 0000-00-00 | No | No | Current |