Ranitidine
- Product NDC
- 49781-026
- 11-digit product format
- 497810026
- Labeler code
- 49781
- Product ID
- 49781-026_4943c1d0-dd17-4785-99bd-bf3dd78461f0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA201745
- Marketing category
- ANDA
- Marketing start
- 2013-09-25
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 75 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 49781-026-30 | 2025-05-12 | C162847 | 48780-1 | 9d75b9d0-3e77-f424-e053-dadaa90a57ce | c2c82f2e-763a-4459-b18f-e2ca8f22f7f7 |
| 49781-026-60 | 2025-05-12 | C162847 | 48780-1 | 9d75b9d0-3e77-f424-e053-dadaa90a57ce | c2c82f2e-763a-4459-b18f-e2ca8f22f7f7 |
| 49781-026-30 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-3e77-f424-e053-dadaa90a57ce | c2c82f2e-763a-4459-b18f-e2ca8f22f7f7 |
| 49781-026-60 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-3e77-f424-e053-dadaa90a57ce | c2c82f2e-763a-4459-b18f-e2ca8f22f7f7 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49781-026-30 | EA - Each | 49781-026 | e72cc486-f8fc-4111-8516-84fab2e842ef | 1 | 2016-01-13 |
| 49781-026-60 | EA - Each | 49781-026 | fe621aaf-f7d3-432a-b43b-8b422d3cbb46 | 1 | 2016-01-13 |