Propranolol Hydrochloride
- Product NDC
- 72789-372
- 11-digit product format
- 727890372
- Labeler code
- 72789
- Product ID
- 72789-372_3cf820d7-b455-5342-e063-6394a90a4f78
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA071972
- Marketing category
- ANDA
- Marketing start
- 2021-06-03
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Propranolol Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROPRANOLOL HYDROCHLORIDE | 40 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F8A3652H1V |
| Rxcui | 856519 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-372-90 | Propranolol Hydrochloride | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-372 | PROPRANOLOL HYDROCHLORIDE TABLET [PD-RX PHARMACEUTICALS, INC.] | 4 | Current NDC, 1 package rows | 20240123_95a2eacd-b6b7-4e92-ae14-52fbee6c6543.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 |
|---|
| 72789-372-90 | 72789037290 | 90 TABLET in 1 BOTTLE, PLASTIC (72789-372-90) | 90 tablet | 2024-01-22 | No | No | Current |