Propranolol Hydrochloride
- Product NDC
- 50090-3296
- 11-digit product format
- 500903296
- Labeler code
- 50090
- Product ID
- 50090-3296_3ea25c09-52af-4344-a455-9e53d04641aa
- 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
- 2016-09-19
- 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 |
|---|
| 50090-3296-1 | Propranolol Hydrochloride | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 6 |
| 50090-3296-6 | Propranolol Hydrochloride | 90 in 1 BOTTLE | TABLET | 90 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3296 | PROPRANOLOL HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 6 | Legacy NDC, 2 package rows | 20190430_ade66290-447c-44c2-bf1f-1d2cdbf80d1c.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 |
|---|
| 50090-3296-1 | 50090329601 | 100 TABLET in 1 BOTTLE, PLASTIC (50090-3296-1) | 100 tablet | 2016-09-19 | 0000-00-00 | No | No | Current |
| 50090-3296-6 | 50090329606 | 90 TABLET in 1 BOTTLE (50090-3296-6) | 90 tablet | 2017-12-01 | 0000-00-00 | No | No | Current |