Rabeprazole Sodium
- Product NDC
- 51991-683
- 11-digit product format
- 519910683
- Labeler code
- 51991
- Product ID
- 51991-683_3dc0927a-7942-4246-811d-ad789aac2cb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- RABEPRAZOLE SODIUM
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Application
- ANDA204237
- Marketing category
- ANDA
- Marketing start
- 2017-06-01
- Marketing end
- 2020-02-28
- Substance
- RABEPRAZOLE SODIUM
- Active strength
- 20 mg/1
- Pharmacologic classes
- Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| e2db08c6-133f-4f4f-afb4-e90a2418d6f6 | Product name | 1 | 20230320 |
| 11ed6f83-cdd2-4637-8379-b1a1d3ae3cde | Product name | 1 | 20181101 |
| 41e5d082-a3b8-4ff4-92a1-6fdf8d5110b4 | Product name | 4 | 20180626 |
| 86c45a79-b9f0-4476-a27c-6e10db098497 | Product name | 1 | 20180125 |
| 9a0b93b8-7081-4ac2-867c-2955b2d759fd | Product name | 2 | 20170909 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51991-683-33 | EA - Each | 51991-683 | fbdd2d08-0b87-4125-9b63-d7a3a068fc5d | 1 | 2017-08-11 |
| 51991-683-90 | EA - Each | 51991-683 | 1fa53219-b4ba-46b2-a45b-2e924342e942 | 1 | 2017-08-11 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 854868 | RABEprazole sodium 20 MG Delayed Release Oral Tablet | PSN | c1910485-1954-4fbe-9717-4cb9e6fe84a2 | 2 |
| 854868 | rabeprazole sodium 20 MG Delayed Release Oral Tablet | SCD | c1910485-1954-4fbe-9717-4cb9e6fe84a2 | 2 |