Esomeprazole Magnesium
- Product NDC
- 43598-469
- 11-digit product format
- 435980469
- Labeler code
- 43598
- Product ID
- 43598-469_3fb729ea-a04a-bfdd-d564-7045771e1247
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Esomeprazole Magnesium
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Dr. Reddys Laboratories Inc
- Application
- ANDA211571
- Marketing category
- ANDA
- Marketing start
- 2020-11-15
- Marketing end
- 0000-00-00
- Substance
- ESOMEPRAZOLE MAGNESIUM
- Active strength
- 20 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 |
|---|
| 43598-469-28 | 43598046928 | 2 BOTTLE in 1 CARTON (43598-469-28) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 2 bottle | 2020-11-15 | 0000-00-00 | No | No | Current |
| 43598-469-42 | 43598046942 | 3 BOTTLE in 1 CARTON (43598-469-42) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2020-11-15 | 0000-00-00 | No | No | Current |
| 43598-469-52 | 43598046952 | 1 BOTTLE in 1 CARTON (43598-469-52) > 14 TABLET, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2020-11-15 | 0000-00-00 | No | No | Current |