Omeprazole Magnesium
- Product NDC
- 43598-813
- 11-digit product format
- 435980813
- Labeler code
- 43598
- Product ID
- 43598-813_4eefad5b-fb8f-d7f1-0138-90a07d45edfa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Omeprazole Magnesium
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Dr. Reddy's Laboratories Inc.
- Application
- ANDA078878
- Marketing category
- ANDA
- Marketing start
- 2018-12-26
- Substance
- OMEPRAZOLE MAGNESIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Omeprazole Magnesium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OMEPRAZOLE MAGNESIUM | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 426QFE7XLK |
| Rxcui | 198051 |
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43598-813 | OMEPRAZOLE MAGNESIUM CAPSULE, DELAYED RELEASE [DR. REDDY'S LABORATORIES INC.] | 4 | Current NDC, Legacy NDC | 20241112_fe0eb905-2042-aed1-a67d-a219e76f679b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43598-813-14 | 43598081314 | 1 BOTTLE in 1 CARTON (43598-813-14) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 1 bottle | 2018-12-26 | 0000-00-00 | No | No | Current |
| 43598-813-33 | 43598081333 | 3 BOTTLE in 1 CARTON (43598-813-33) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE | 3 bottle | 2018-12-26 | 0000-00-00 | No | No | Current |