Home NDC 0527-1170 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
Product NDC 0527-1170
11-digit product format 005271170
Labeler code 0527
Product ID 0527-1170_7d6498f1-eb15-4601-861d-5cc81862292a
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE
Dosage form TABLET
Route ORAL
Labeler Lannett Company, Inc.
Application ANDA085372
Marketing category ANDA
Marketing start 1978-02-21
Marketing end 0000-00-00
Substance ATROPINE; DIPHENOXYLATE
Active strength 0 mg/1; mg/1
Pharmacologic classes Anticholinergic [EPC], Antidiarrheal [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
DEA schedule CV
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 36 matching rows.
View current auxiliary records. · View the auxiliary file history.
Source provenance: Browse the complete Orange Book source catalog · source snapshot 1 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982
Therapeutic equivalence codes# Current TE-code rows page 1 of 1 · 1 matching rows.
Application-product, TE code table Application-product TE code A085372-001 AA
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.
Product history page 1 of 2 · 41 observed 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 2026-02-19 14:30 UTC 2026-02 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 301d65b070ca…2024-06-18 03:08 UTC · 5 captures of this ZIP 2024-06 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 1e350fbaab3a…2024-05-31 18:47 UTC 2024-05 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 8072bd15b7f6…2022-06-29 02:47 UTC · 2 captures of this ZIP 2022-06 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 5c6f7cd8ea54…2022-04-08 23:34 UTC 2022-04 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 5d02ea3f76ae…2022-04-04 05:41 UTC 2022-04 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 4b0b4de00fa7…2019-12-13 00:20 UTC 2019-12 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 74a2ff9319b5…2022-03-09 01:35 UTC 2022-03 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 bb7c543d1eb4…2021-12-28 21:50 UTC 2021-12 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 782e0a99824c…2021-05-05 16:15 UTC · 3 captures of this ZIP 2021-05 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 87673890dc5c…2021-03-12 10:30 UTC 2021-03 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 5aa47cf7b7d7…2020-12-22 03:56 UTC 2020-12 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 8869cabd3fbd…2020-11-12 02:37 UTC 2020-11 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 c0c555d07b60…2019-12-14 00:12 UTC 2019-12 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 3f01610625f2…2019-09-15 20:21 UTC 2019-09 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 b00525d2431f…2019-07-19 19:46 UTC 2019-07 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 ea99ee380514…2024-03-16 18:09 UTC · 4 captures of this ZIP 2024-03 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 6a51e52b5d6a…2024-02-18 07:12 UTC 2024-02 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 1c564ffb4f44…2023-12-20 04:57 UTC 2023-12 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 ea1830bbd6c7…2023-11-28 05:40 UTC · 2 captures of this ZIP 2023-11 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 a72a2bbeb626…2023-10-25 00:34 UTC · 2 captures of this ZIP 2023-10 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 9b2671bbb829…2023-07-15 15:27 UTC · 2 captures of this ZIP 2023-07 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 a67488948f0b…2023-06-13 01:57 UTC · 3 captures of this ZIP 2023-06 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 3f0d92c62455…2023-05-13 08:27 UTC 2023-05 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 053a50430f4f…2023-01-26 05:58 UTC 2023-01 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 3bdfa0b2c4d7…2022-11-12 20:34 UTC · 5 captures of this ZIP 2022-11 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 3a93d1ddd44b…2022-10-28 04:53 UTC 2022-10 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 f41ea6bd6efb…2022-09-29 23:25 UTC 2022-09 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A085372-001 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE 0.025MG;2.5MG TABLET / ORAL AA Approved before 1982 cb3db0bc1861…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 2 · 41 observed states.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# NDC, Effective, Action table NDC Effective Action Document Indexing SPL Related label 0527-1170-01 2024-01-30 C162847 48780-1 1030e365-584c-111a-e063-dadaa90a10e2 Diphenoxylate Hydrochloride and Atropine Sulfate Tablets, USP, for oral use, CV 0527-1170-05 2024-01-30 C162847 48780-1 1030e365-584c-111a-e063-dadaa90a10e2 Diphenoxylate Hydrochloride and Atropine Sulfate Tablets, USP, for oral use, CV 0527-1170-10 2024-01-30 C162847 48780-1 1030e365-584c-111a-e063-dadaa90a10e2 Diphenoxylate Hydrochloride and Atropine Sulfate Tablets, USP, for oral use, CV
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded atropine sulfate ACTIVE INGREDIENT 03J5ZE7KA5 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE (DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE) TABLET [LANNETT CO., INC.] 3 diphenoxylate hydrochloride ACTIVE INGREDIENT W24OD7YW48 DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE (DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE) TABLET [LANNETT CO., INC.] 3 atropine ACTIVE MOIETY 7C0697DR9I DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE (DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE) TABLET [LANNETT CO., INC.] 3 diphenoxylate ACTIVE MOIETY 73312P173G DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE (DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE) TABLET [LANNETT CO., INC.] 3 acacia INACTIVE INGREDIENT DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE (DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE) TABLET [LANNETT CO., INC.] 3 calcium stearate INACTIVE INGREDIENT 776XM7047L DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE (DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE) TABLET [LANNETT CO., INC.] 3 corn starch INACTIVE INGREDIENT DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE (DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE) TABLET [LANNETT CO., INC.] 3 lactose monohydrate INACTIVE INGREDIENT EWQ57Q8I5X DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE (DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE) TABLET [LANNETT CO., INC.] 3 methylcellulose INACTIVE INGREDIENT DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE (DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE) TABLET [LANNETT CO., INC.] 3
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0527-1170-01 00527117001 100 TABLET in 1 BOTTLE (0527-1170-01) 100 tablet 1978-02-21 0000-00-00 No No Current 0527-1170-05 00527117005 500 TABLET in 1 BOTTLE (0527-1170-05) 500 tablet 1978-02-21 0000-00-00 No No Current 0527-1170-10 00527117010 1000 TABLET in 1 BOTTLE (0527-1170-10) 1000 tablet 1978-02-21 0000-00-00 No No Current