Propranolol Hydrochloride
- Product NDC
- 50090-3953
- 11-digit product format
- 500903953
- Labeler code
- 50090
- Product ID
- 50090-3953_51bd2f0d-463e-4694-8e4f-bc7ff4cb57c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA070176
- Marketing category
- ANDA
- Marketing start
- 1986-05-13
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [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 |
|---|
| 50090-3953-1 | Propranolol Hydrochloride | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 50090-3953-6 | Propranolol Hydrochloride | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3953 | PROPRANOLOL HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20190501_7ccdded1-6342-492f-a18e-9a3da3af5a8b.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 |
|---|
| 50090-3953-1 | 50090395301 | 100 TABLET in 1 BOTTLE (50090-3953-1) | 100 tablet | 2018-12-11 | 0000-00-00 | No | No | Current |
| 50090-3953-6 | 50090395306 | 90 TABLET in 1 BOTTLE, PLASTIC (50090-3953-6) | 90 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |