Ranitidine
- Product NDC
- 50436-0253
- 11-digit product format
- 504360253
- Labeler code
- 50436
- Product ID
- 50436-0253_86f114a3-07cd-4a0a-8048-5aa2d832daaf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077824
- Marketing category
- ANDA
- Marketing start
- 2009-12-16
- Marketing end
- 0000-00-00
- Substance
- RANITIDINE HYDROCHLORIDE
- Active strength
- 150 mg/1
- Pharmacologic classes
- Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50436-0253-1 | Ranitidine | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 50436-0253-2 | Ranitidine | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
| 50436-0253-6 | Ranitidine | 180 in 1 BOTTLE | TABLET | 180 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0253 | RANITIDINE TABLET [UNIT DOSE SERVICES] | 3 | Legacy NDC, 3 package rows | 20190514_8b65ebf4-e1a7-4592-8652-93dc5e011437.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0253-1 | 50436025301 | 30 in 1 BOTTLE | Historical |
| 50436-0253-2 | 50436025302 | 60 in 1 BOTTLE | Historical |
| 50436-0253-6 | 50436025306 | 180 in 1 BOTTLE | Historical |