Loratadine

Product NDC: 70010-162
11-digit product format: 700100162
Labeler code: 70010
Product ID: 70010-162_346155e4-f155-2f14-e063-6294a90ac61f
Type: HUMAN OTC DRUG
Nonproprietary name: Loratadine
Dosage form: TABLET
Route: ORAL
Labeler: Granules Pharmaceuticals Inc.
Application: ANDA210722
Marketing category: ANDA
Marketing start: 2020-01-01
Substance: LORATADINE
Active strength: 10 mg/1
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 42.

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
A210722-001	LORATADINE	LORATADINE	10MG	TABLET / ORAL			2019-12-23

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	Approval date	Source SHA-256
2026-08-18 06:07:40	2026-07	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`4b0b4de00fa7…`
2022-03-09 01:35 UTC	2022-03	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`c0c555d07b60…`
2024-03-16 18:09 UTC · 4 captures of this ZIP	2024-03	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`6a51e52b5d6a…`
2024-02-18 07:12 UTC	2024-02	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`1c564ffb4f44…`
2023-12-20 04:57 UTC	2023-12	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`ea1830bbd6c7…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`a72a2bbeb626…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`9b2671bbb829…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`a67488948f0b…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`3f0d92c62455…`
2023-05-13 08:27 UTC	2023-05	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`053a50430f4f…`
2023-01-26 05:58 UTC	2023-01	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`3bdfa0b2c4d7…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`3a93d1ddd44b…`
2022-10-28 04:53 UTC	2022-10	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`f41ea6bd6efb…`
2022-09-29 23:25 UTC	2022-09	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`e64feba35796…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`cb3db0bc1861…`
2026-07-26 02:55 UTC · 3 captures of this ZIP	2026-06	A210722-001	LORATADINE	10MG	TABLET / ORAL	2019-12-23	`a50c72e98297…`

Additional Listing Data#

Finished product: Yes
Brand name base: Loratadine
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
LORATADINE	10 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
7AJO3BO7QN	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
311372	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
d15add22-bc2d-9730-e053-2a95a90acd3f	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
70010-162-01	Loratadine	100 in 1 BOTTLE	TABLET	100	5
70010-162-03	Loratadine	30 in 1 BOTTLE	TABLET	30	5
70010-162-34	Loratadine	300 in 1 BOTTLE	TABLET	300	5

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70010-162-01	EA - Each	70010-162	590b49a0-7416-4a5b-9ef6-cdc10a4b3a3f	1	2021-12-08
70010-162-34	EA - Each	70010-162	9d40ed54-0327-411e-9606-1ffef0f56c90	1	2022-09-12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70010-162	LORATADINE TABLET [GRANULES PHARMACEUTICALS INC.]	5	Current NDC, Legacy NDC, 3 package rows	20250508_d15add22-bc2d-9730-e053-2a95a90acd3f.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 2 · 40 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Allergy Relief	LORATADINE	Dr. Reddy's Laboratories Inc.	44da36d2-1881-e779-d3a2-13ea828f9240	2026-07-15	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Loratadine	LORATADINE	St. Mary's Medical Park Pharmacy	2bc586e4-5297-44cf-e063-6294a90a531d	2026-06-29	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Loratadine	LORATADINE	Preferred Pharmaceuticals Inc.	c6144a33-6b33-4aca-86e5-a3f688b8b317	2026-05-28	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Allergy Relief	LORATADINE	Grocery Outlet, Inc	441cfa86-a812-f67f-e063-6394a90a2118	2026-05-21	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Loratadine	LORATADINE	NuCare Pharmaceuticals,Inc.	16f00a3a-0777-f70c-e063-6294a90a71c9	2026-04-06	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
ALLERGY RELIEF 10 mg	LORATADINE	TWIN MED LLC	d943f548-aa0d-4476-e053-2a95a90a7bd4	2026-04-01	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Dr Simi All Day Allergy Relief	LORATADINE	Farmacias De Similares TX LLC	3c5b2eaa-24da-3314-e063-6294a90a5b21	2026-02-26	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Loratadine	LORATADINE	GRANULES USA, INC.	c3c9bc45-7ed5-abf4-e053-2995a90a40ff	2025-12-22	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Loratadine	LORATADINE	Safeway, Inc	f2a2a754-0170-e37c-e053-2a95a90a4dca	2025-12-19	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Loratadine 10mg	LORATADINE 10MG	Meijer	181b7dd1-ddc4-e799-e063-6294a90a9faa	2025-12-19	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Loratadine	LORATADINE	Walgreens	fd796139-ea9f-f4db-e053-6394a90acdf3	2025-12-19	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Allergy Relief	LORATADINE	Valu Merchandisers Company	05927511-6b7a-4e29-96b4-3043493acf11	2025-12-11	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
CAREALL Allergy Relief	LORATADINE	New World Imports	4d15d926-9564-4bef-b8a9-768af7a0ab6a	2025-12-01	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Green Guard 24 Hour Allergy Relief	LORATADINE	Unifirst First Aid Corporation	f98a45fd-cda8-4884-e053-6294a90a57b5	2025-11-21	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Allergy Relief	LORATADINE	WinCo Foods, LLC	3dea627d-4b0c-e077-e063-6394a90a15a0	2025-11-03	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
McKesson Loratadine	LORATADINE 10 MG	McKesson Medical Surgical	c6a3056e-792e-52a4-e053-2a95a90a8361	2025-10-23	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
First Aid Direct Allergy Relief	LORATADINE TABLETS	Cintas Corporation	6b43e5a5-30a8-46ca-a44d-1e1abf567b51	2025-09-23	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Loratadine	LORATADINE	Granules India Limited	9bae1ba3-c0da-23a2-e053-2a95a90a58ed	2025-08-01	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Curist Allergy Relief	LORATADINE 10 MG	Little Pharma, Inc.	0c53cf0f-7682-a422-e063-6394a90ab764	2025-06-15	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722
Loratadine	LORATADINE	Bryant Ranch Prepack	0d74af21-3ef7-418b-a2ef-78737b0af288	2025-06-13	Warnings	Exact identifier application applno (ANDA): 210722 application number: ANDA210722

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
7AJO3BO7QN	LORATADINE	79794-75-5	LORATADINE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
311372	loratadine 10 MG 24HR Oral Tablet	PSN	d15add22-bc2d-9730-e053-2a95a90acd3f	5
311372	loratadine 10 MG Oral Tablet	SCD	d15add22-bc2d-9730-e053-2a95a90acd3f	5
311372	loratadine 10 MG 24 HR Oral Tablet	SY	d15add22-bc2d-9730-e053-2a95a90acd3f	5
311372	loratadine 10 MG 24HR Oral Tablet	PSN	16f00a3a-0777-f70c-e063-6294a90a71c9	3
311372	loratadine 10 MG 24HR Oral Tablet	PSN	c6144a33-6b33-4aca-86e5-a3f688b8b317	3
311372	loratadine 10 MG Oral Tablet	SCD	16f00a3a-0777-f70c-e063-6294a90a71c9	3
311372	loratadine 10 MG Oral Tablet	SCD	c6144a33-6b33-4aca-86e5-a3f688b8b317	3
311372	loratadine 10 MG 24 HR Oral Tablet	SY	16f00a3a-0777-f70c-e063-6294a90a71c9	3
311372	loratadine 10 MG 24 HR Oral Tablet	SY	c6144a33-6b33-4aca-86e5-a3f688b8b317	3
311372	loratadine 10 MG 24HR Oral Tablet	PSN	a5d54183-06a9-4ae1-93b9-e9a2e03ad42b	2
311372	loratadine 10 MG 24HR Oral Tablet	PSN	2bc586e4-5297-44cf-e063-6294a90a531d	2
311372	loratadine 10 MG 24HR Oral Tablet	PSN	0d74af21-3ef7-418b-a2ef-78737b0af288	2
311372	loratadine 10 MG Oral Tablet	SCD	a5d54183-06a9-4ae1-93b9-e9a2e03ad42b	2
311372	loratadine 10 MG Oral Tablet	SCD	0d74af21-3ef7-418b-a2ef-78737b0af288	2
311372	loratadine 10 MG Oral Tablet	SCD	2bc586e4-5297-44cf-e063-6294a90a531d	2
311372	loratadine 10 MG 24 HR Oral Tablet	SY	a5d54183-06a9-4ae1-93b9-e9a2e03ad42b	2
311372	loratadine 10 MG 24 HR Oral Tablet	SY	2bc586e4-5297-44cf-e063-6294a90a531d	2
311372	loratadine 10 MG 24 HR Oral Tablet	SY	0d74af21-3ef7-418b-a2ef-78737b0af288	2

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70010-162-01	70010016201	100 TABLET in 1 BOTTLE (70010-162-01)	100 tablet	2021-11-17	0000-00-00	No	No	Current
70010-162-03	70010016203	30 TABLET in 1 BOTTLE (70010-162-03)	30 tablet	2022-05-01		No	No	Current
70010-162-34	70010016234	300 TABLET in 1 BOTTLE (70010-162-34)	300 tablet	2022-05-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Loratadine Tablets, 10 mg	St. Mary's Medical Park Pharmacy	2026-06-29	HUMAN OTC DRUG LABEL	3
Loratadine Tablets, 10 mg	Preferred Pharmaceuticals Inc.	2026-05-28	HUMAN OTC DRUG LABEL	3
Loratadine Tablets, 10 mg	NuCare Pharmaceuticals,Inc.	2026-04-06	HUMAN OTC DRUG LABEL	3
Loratadine Tablets, 10 mg	Bryant Ranch Prepack	2025-06-13	HUMAN PRESCRIPTION DRUG LABEL	2
Loratadine Tablets, 10 mg	Bryant Ranch Prepack	2025-06-13	HUMAN OTC DRUG LABEL	2
Loratadine Tablets, 10 mg	Granules Pharmaceuticals Inc.	2025-05-05	HUMAN OTC DRUG LABEL	5