lansoprazole
- Product NDC
- 45802-245
- 11-digit product format
- 458020245
- Labeler code
- 45802
- Product ID
- 45802-245_9aaa8c78-11a3-4e9a-b044-9eda38fa6620
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Padagis Israel Pharmaceuticals Ltd
- Application
- ANDA202319
- Marketing category
- ANDA
- Marketing start
- 2012-08-07
- Marketing end
- 0000-00-00
- Substance
- LANSOPRAZOLE
- Active strength
- 15 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 |
|---|
| 45802-245-01 | 45802024501 | 1 BOTTLE in 1 CARTON (45802-245-01) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2012-08-07 | 0000-00-00 | No | No | Current |
| 45802-245-02 | 45802024502 | 2 BOTTLE in 1 CARTON (45802-245-02) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 2 bottle | 2012-08-07 | 0000-00-00 | No | No | Current |
| 45802-245-03 | 45802024503 | 3 BOTTLE in 1 CARTON (45802-245-03) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2012-08-07 | 0000-00-00 | No | No | Current |