Ranitidine
- Product NDC
- 50090-2740
- 11-digit product format
- 500902740
- Labeler code
- 50090
- Product ID
- 50090-2740_8f3aac51-2871-462f-a421-83666d72f869
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ranitidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078542
- Marketing category
- ANDA
- Marketing start
- 2008-11-19
- 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
- 2022-12-31
- 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 |
|---|
| 50090-2740-0 | Ranitidine | 14 in 1 BOTTLE | TABLET, FILM COATED | 14 | | 10 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2740 | RANITIDINE TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 10 | Legacy NDC, 1 package rows | 20210302_80069a62-6022-4070-b466-8d7bbe49dc6f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-2740-0 | 50090274000 | 14 TABLET, FILM COATED in 1 BOTTLE (50090-2740-0) | 2017-01-02 | 0000-00-00 | No | No | Current |