Propranolol Hydrochloride
- Product NDC
- 51655-302
- 11-digit product format
- 516550302
- Labeler code
- 51655
- Product ID
- 51655-302_48eadbc7-2351-2bb6-e063-6294a90a067d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- propranolol hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA070221
- Marketing category
- ANDA
- Marketing start
- 2020-05-19
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Propranolol Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROPRANOLOL HYDROCHLORIDE | 20 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F8A3652H1V |
| Rxcui | 856457 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-302-26 | Propranolol Hydrochloride | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-302 | PROPRANOLOL HYDROCHLORIDE TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 3 | Current NDC, 1 package rows | 20241219_f2b8b894-d887-c4ee-e053-2995a90a0c0b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 51655-302-26 | 51655030226 | 90 TABLET in 1 BOTTLE, PLASTIC (51655-302-26) | 90 tablet | 2020-05-19 | No | No | Current |