Propranolol Hydrochloride
- Product NDC
- 53808-1126
- 11-digit product format
- 538081126
- Labeler code
- 53808
- Product ID
- 53808-1126_edc27a6e-47a2-4894-8068-b4f9daa48594
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DOH CENTRAL PHARMACY
- Application
- ANDA070176
- Marketing category
- ANDA
- Marketing start
- 2017-10-09
- 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 |
|---|
| 53808-1126-1 | Propranolol Hydrochloride | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-1126 | PROPRANOLOL HYDROCHLORIDE TABLET [DOH CENTRAL PHARMACY] | 1 | Legacy NDC, 1 package rows | 20190125_500d1770-2695-40c8-99a4-abf3fdf8b236.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 |
|---|
| 53808-1126-1 | 53808112601 | 30 TABLET in 1 BLISTER PACK (53808-1126-1) | 30 tablet | 2017-10-09 | 0000-00-00 | No | No | Current |