Lansoprazole
- Product NDC
- 0363-4069
- 11-digit product format
- 003634069
- Labeler code
- 0363
- Product ID
- 0363-4069_c83549f5-fc2d-47c0-ab94-b64d017bfd48
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Lansoprazole
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- ANDA202319
- Marketing category
- ANDA
- Marketing start
- 2018-06-26
- 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 |
|---|
| 0363-4069-01 | 00363406901 | 1 BOTTLE in 1 CARTON (0363-4069-01) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2018-06-26 | 0000-00-00 | No | No | Current |
| 0363-4069-02 | 00363406902 | 2 BOTTLE in 1 CARTON (0363-4069-02) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 2 bottle | 2018-06-26 | 0000-00-00 | No | No | Current |
| 0363-4069-03 | 00363406903 | 3 BOTTLE in 1 CARTON (0363-4069-03) > 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2018-06-26 | 0000-00-00 | No | No | Current |