Home NDC 42689-014-01 Propranolol Hydrochloride
Product NDC 42689-014
Requested package NDC 42689-014-01
11-digit product format 426890014
Labeler code 42689
Product ID 42689-014_81548a65-4cc7-4e02-9846-590737a74469
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Propranolol Hydrochloride
Dosage form CAPSULE, EXTENDED RELEASE
Route ORAL
Labeler Nortec Development Associates, Inc
Application ANDA078065
Marketing category ANDA
Marketing start 2015-05-01
Marketing end 0000-00-00
Substance PROPRANOLOL HYDROCHLORIDE
Active strength 160 mg/1
Pharmacologic classes Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 4 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A078065-001 PROPRANOLOL HYDROCHLORIDE PROPRANOLOL HYDROCHLORIDE 60MG CAPSULE, EXTENDED RELEASE / ORAL AB 2007-01-26 A078065-002 PROPRANOLOL HYDROCHLORIDE PROPRANOLOL HYDROCHLORIDE 80MG CAPSULE, EXTENDED RELEASE / ORAL AB 2007-01-26 A078065-003 PROPRANOLOL HYDROCHLORIDE PROPRANOLOL HYDROCHLORIDE 120MG CAPSULE, EXTENDED RELEASE / ORAL AB 2007-01-26 A078065-004 PROPRANOLOL HYDROCHLORIDE PROPRANOLOL HYDROCHLORIDE 160MG CAPSULE, EXTENDED RELEASE / ORAL AB 2007-01-26
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 4 matching rows.
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-01 22:54:32 2026-06 A078065-001 PROPRANOLOL HYDROCHLORIDE 60MG CAPSULE, EXTENDED RELEASE / ORAL AB 2007-01-26 a50c72e98297…2026-08-01 22:54:32 2026-06 A078065-002 PROPRANOLOL HYDROCHLORIDE 80MG CAPSULE, EXTENDED RELEASE / ORAL AB 2007-01-26 a50c72e98297…2026-08-01 22:54:32 2026-06 A078065-003 PROPRANOLOL HYDROCHLORIDE 120MG CAPSULE, EXTENDED RELEASE / ORAL AB 2007-01-26 a50c72e98297…2026-08-01 22:54:32 2026-06 A078065-004 PROPRANOLOL HYDROCHLORIDE 160MG CAPSULE, EXTENDED RELEASE / ORAL AB 2007-01-26 a50c72e98297…
Observed Orange Book normalized TE history# 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 42689-014-01 Propranolol Hydrochloride 100 in 1 BOTTLE CAPSULE, EXTENDED RELEASE 100 5 42689-014-10 Propranolol Hydrochloride 1000 in 1 BOTTLE CAPSULE, EXTENDED RELEASE 1000 5
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Propranolol Hydrochloride ACTIVE INGREDIENT F8A3652H1V PROPRANOLOL HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTEC DEVELOPMENT ASSOCIATES, INC] 1 PROPRANOLOL ACTIVE MOIETY 9Y8NXQ24VQ PROPRANOLOL HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTEC DEVELOPMENT ASSOCIATES, INC] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U PROPRANOLOL HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTEC DEVELOPMENT ASSOCIATES, INC] 1 ETHYLCELLULOSE (45 MPA.S) INACTIVE INGREDIENT V7AD894FAZ PROPRANOLOL HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTEC DEVELOPMENT ASSOCIATES, INC] 1 FD&C BLUE NO. 1 INACTIVE INGREDIENT H3R47K3TBD PROPRANOLOL HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTEC DEVELOPMENT ASSOCIATES, INC] 1 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA PROPRANOLOL HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTEC DEVELOPMENT ASSOCIATES, INC] 1 GELATIN INACTIVE INGREDIENT 2G86QN327L PROPRANOLOL HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTEC DEVELOPMENT ASSOCIATES, INC] 1 HYPROMELLOSE 2910 (5 MPA.S) INACTIVE INGREDIENT R75537T0T4 PROPRANOLOL HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTEC DEVELOPMENT ASSOCIATES, INC] 1 TITANIUM DIOXIDE INACTIVE INGREDIENT 15FIX9V2JP PROPRANOLOL HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTEC DEVELOPMENT ASSOCIATES, INC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 42689-014 PROPRANOLOL HYDROCHLORIDE CAPSULE, EXTENDED RELEASE [NORTEC DEVELOPMENT ASSOCIATES, INC] 5 Legacy NDC, 2 package rows 20241204_b756f602-62c9-41ef-a934-834ac81b46ae.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 42689-014-01 42689001401 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (42689-014-01) 2015-05-01 0000-00-00 No No Current