Propranolol Hydrochloride
- Product NDC
- 68151-2013
- 11-digit product format
- 681512013
- Labeler code
- 68151
- Product ID
- 68151-2013_56a92945-fac8-44ca-b3a1-5262cf5c0409
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Propranolol Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Carilion Materials Management
- Application
- ANDA070175
- Marketing category
- ANDA
- Marketing start
- 1986-05-13
- Marketing end
- 0000-00-00
- Substance
- PROPRANOLOL HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 68151-2013-1 | Propranolol Hydrochloride | 1 in 1 BOTTLE | TABLET | 1 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68151-2013 | PROPRANOLOL HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT] | 4 | Legacy NDC, 1 package rows | 20150625_3b21bec3-3b6a-4d6d-adf7-11dedbd37abe.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 68151-2013-1 | 68151201301 | 1 in 1 BOTTLE | Historical |