Esomeprazole Magnesium
- Product NDC
- 0363-0305
- 11-digit product format
- 003630305
- Labeler code
- 0363
- Product ID
- 0363-0305_5d9c254d-460c-3c1d-aac2-bf06c4d5ba34
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Walgreens Company
- Application
- ANDA211571
- Marketing category
- ANDA
- Marketing start
- 2019-12-31
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE MAGNESIUM
- Active strength
- 20 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 |
|---|---|---|---|---|---|---|---|---|
| 0363-0305-14 | 00363030514 | 1 BOTTLE in 1 CARTON (0363-0305-14) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2019-12-31 | 0000-00-00 | No | No | Current |
| 0363-0305-42 | 00363030542 | 3 BOTTLE in 1 CARTON (0363-0305-42) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2019-12-31 | 0000-00-00 | No | No | Current |