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NDC 42689-0014-10 Propranolol Hydrochloride 160 mg/1 Details
Propranolol Hydrochloride 160 mg/1
Propranolol Hydrochloride is a ORAL CAPSULE, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Nortec Development Associates, Inc. The primary component is PROPRANOLOL HYDROCHLORIDE.
Product Information
| NDC | 42689-0014 |
|---|---|
| Product ID | 42689-014_0a5bc268-a231-1779-e063-6294a90aa769 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Propranolol Hydrochloride |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Propranolol Hydrochloride |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CAPSULE, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 160 |
| Active Ingredient Units | mg/1 |
| Substance Name | PROPRANOLOL HYDROCHLORIDE |
| Labeler Name | Nortec Development Associates, Inc |
| Pharmaceutical Class | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA078065 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 42689-0014-10 (42689001410)
| NDC Package Code | 42689-014-10 |
|---|---|
| Billing NDC | 42689001410 |
| Package | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42689-014-10) |
| Marketing Start Date | 2015-05-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |