| NDC Code | 60687-248-32 |
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| Package Description | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-248-32) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-248-33) |
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| Product NDC | 60687-248 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Propranolol Hydrochloride |
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| Non-Proprietary Name | Propranolol Hydrochloride |
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| Dosage Form | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20170201 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078703 |
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| Manufacturer | American Health Packaging |
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| Substance Name | PROPRANOLOL HYDROCHLORIDE |
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| Strength | 160 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
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