Propranolol Hydrochloride
- Product NDC
- 50090-2829
- 11-digit product format
- 500902829
- Labeler code
- 50090
- Product ID
- 50090-2829_0d79ff12-b962-4348-ae2d-f40a2b5f44dc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA070221
- Marketing category
- ANDA
- Marketing start
- 2010-06-21
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-2829-0 | Propranolol Hydrochloride | 1 in 1 BLISTER PACK | TABLET | 1 | | 17 |
| 50090-2829-0 | Propranolol Hydrochloride | 32 in 1 BOX, UNIT-DOSE | TABLET | 32 | | 17 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-2829 | PROPRANOLOL HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 17 | Legacy NDC, 2 package rows | 20221208_1a821300-3d6c-4990-ae6d-771d549adddf.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 |
|---|
| 50090-2829-0 | 50090282900 | 32 BLISTER PACK in 1 BOX, UNIT-DOSE (50090-2829-0) > 1 TABLET in 1 BLISTER PACK | 32 blister pack | 2017-02-01 | 0000-00-00 | No | No | Current |