Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate

Product NDC: 71335-1725
11-digit product format: 713351725
Labeler code: 71335
Product ID: 71335-1725_8a668a34-0be3-4aa9-8c87-3e9648f480cf
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate
Dosage form: TABLET
Route: SUBLINGUAL
Labeler: Bryant Ranch Prepack
Application: ANDA207000
Marketing category: ANDA
Marketing start: 2017-12-13
Substance: BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE
Active strength: 8; 2 mg/1; mg/1
Pharmacologic classes: Opioid Antagonist [EPC], Opioid Antagonists [MoA], Partial Opioid Agonist [EPC], Partial Opioid Agonists [MoA]
DEA schedule: CIII
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 2 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB		2017-12-13
A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB		2017-12-13

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 2 matching rows.

Application-product, TE code table
Application-product	TE code
A207000-001	AB
A207000-002	AB

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 3 · 82 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Product TE source text	Approval date	Source SHA-256
2026-02-19 14:30 UTC	2026-02	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	A207000-001	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 2MG BASE;EQ 0.5MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	A207000-002	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE	EQ 8MG BASE;EQ 2MG BASE	TABLET / SUBLINGUAL	AB	2017-12-13	`782e0a99824c…`

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 3 · 82 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2026-02-19 14:30 UTC	2026-02	A207000-001	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A207000-002	AB	1	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A207000-001	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A207000-002	AB	1	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A207000-001	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A207000-002	AB	1	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A207000-001	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A207000-002	AB	1	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A207000-001	AB	1	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A207000-002	AB	1	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A207000-001	AB	1	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A207000-002	AB	1	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A207000-001	AB	1	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A207000-002	AB	1	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A207000-001	AB	1	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A207000-002	AB	1	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A207000-001	AB	1	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A207000-002	AB	1	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A207000-001	AB	1	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A207000-002	AB	1	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A207000-001	AB	1	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A207000-002	AB	1	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A207000-001	AB	1	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A207000-002	AB	1	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A207000-001	AB	1	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A207000-002	AB	1	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A207000-001	AB	1	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	A207000-002	AB	1	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A207000-001	AB	1	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A207000-002	AB	1	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A207000-001	AB	1	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	A207000-002	AB	1	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A207000-001	AB	1	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	A207000-002	AB	1	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	A207000-001	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	A207000-002	AB	1	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	A207000-001	AB	1	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	A207000-002	AB	1	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	A207000-001	AB	1	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	A207000-002	AB	1	`782e0a99824c…`

Additional Listing Data#

Finished product: Yes
Brand name base: Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
BUPRENORPHINE HYDROCHLORIDE	8 mg/1
NALOXONE HYDROCHLORIDE DIHYDRATE	2 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
56W8MW3EN1	Internal UNII lookup
5Q187997EE	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
351267	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
b9b5b1d5-482e-42ad-aabd-869e9ade5126	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
68654759-f50b-79ef-24c5-544d94fe7d87	Product name	3	20251114
c955d208-c333-9bd7-be34-d7e12986d44e	Product name	6	20250626
e5f98bfa-66d5-4c3a-b22d-9543d3bee304	Product name	1	20250204
caa6391e-3db3-c912-335f-61b5fc00aa12	Product name	9	20240110
08a295bb-88df-4ab0-a120-a75a789a74f1	Product name	1	20231013
65a3bc34-04ff-4cf1-aad9-c7d92a062f6d	Product name	1	20231003
e951cdf3-f269-4d97-a7d5-c1c3d7283a7d	Product name	3	20230313
ab841ac7-728a-4fc9-be0a-35b96cecbf39	Product name	4	20230306
100316cc-94a9-474e-97ad-9b5c6ddec605	Product name	5	20230125
f327b80c-8fa2-404b-838a-df3eec141cf2	Product name	1	20221212
d4aa2fcf-79c3-4b5f-a00e-1a8e26e00119	Product name	1	20220511
539bc5d3-546b-4af6-9c31-058ce6c459d3	Product name	2	20220210
b871fccd-1de6-4c7f-b9e5-045304641ee6	Product name	8	20220118
43b1efe2-1425-4b3e-b3a2-57d40f8478b9	Product name	1	20211026
31e16ab2-c562-4617-a3e8-ed285320e16e	Product name	1	20180201
4c23a34c-e8fc-424c-8fa0-ee064ba6eaef	Product name	1	20170706
a5920611-4285-f024-69b9-39ff338b81ea	Product name	5	20170609
0b8c7273-1da3-495f-909a-7cf1e96d2361	Product name	1	20161212
3df867ed-9d48-45cf-bded-1394beaea0b1	Product name	3	20161206
973da5bf-b1f9-4de0-81ee-7ca066c98ca4	Product name	1	20160712
8a245632-e24f-4ccc-b671-995d89c96ebc	Product name	1	20141203

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
71335-1725-0	Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	42 in 1 BOTTLE	TABLET	42	107
71335-1725-1	Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	30 in 1 BOTTLE	TABLET	30	107
71335-1725-2	Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	60 in 1 BOTTLE	TABLET	60	107
71335-1725-3	Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	90 in 1 BOTTLE	TABLET	90	107
71335-1725-4	Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	120 in 1 BOTTLE	TABLET	120	107
71335-1725-5	Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	14 in 1 BOTTLE, PLASTIC	TABLET	14	107
71335-1725-6	Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	28 in 1 BOTTLE, PLASTIC	TABLET	28	107
71335-1725-7	Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	6 in 1 BOTTLE, PLASTIC	TABLET	6	107
71335-1725-8	Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	10 in 1 BOTTLE, PLASTIC	TABLET	10	107
71335-1725-9	Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	21 in 1 BOTTLE, PLASTIC	TABLET	21	107

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71335-1725-1	EA - Each	71335-1725	a90e63b1-cac7-4672-af91-cbaa34eec6ee	1	2022-10-06
71335-1725-2	EA - Each	71335-1725	de161d5a-b02d-4a15-a385-4100a146dd56	1	2022-10-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71335-1725	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE DIHYDRATE TABLET [BRYANT RANCH PREPACK]	106	Current NDC, Legacy NDC, 10 package rows	20240410_b9b5b1d5-482e-42ad-aabd-869e9ade5126.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 1 · 4 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE DIHYDRATE	SpecGx LLC	62abde41-46cb-4e90-a798-23d6531bf9aa	2026-06-10	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 207000 application number: ANDA207000
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE DIHYDRATE	Bryant Ranch Prepack	b9b5b1d5-482e-42ad-aabd-869e9ade5126	2026-05-14	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 207000 application number: ANDA207000 ndc (product): 71335-1725
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE DIHYDRATE	Unit Dose Solutions, Inc.	4f979409-f9a2-d3a2-e063-6394a90accd0	2026-04-16	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 207000 application number: ANDA207000
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE DIHYDRATE	Clinical Solutions Wholesale, LLC	273b79ac-2c62-4407-9cd1-2a2964ef13ba	2024-01-09	Warnings, Adverse reactions	Exact identifier application applno (ANDA): 207000 application number: ANDA207000

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
56W8MW3EN1	BUPRENORPHINE HYDROCHLORIDE	53152-21-9	BUPRENORPHINE HYDROCHLORIDE
5Q187997EE	NALOXONE HYDROCHLORIDE DIHYDRATE	51481-60-8	NALOXONE HYDROCHLORIDE DIHYDRATE

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
351267	buprenorphine HCl 8 MG / naloxone HCl 2 MG Sublingual Tablet	PSN	b9b5b1d5-482e-42ad-aabd-869e9ade5126	107
351267	buprenorphine 8 MG / naloxone 2 MG Sublingual Tablet	SCD	b9b5b1d5-482e-42ad-aabd-869e9ade5126	107
351267	buprenorphine 8 MG (as buprenorphine HCl) / naloxone 2 MG (as naloxone HCl) Sublingual Tablet	SY	b9b5b1d5-482e-42ad-aabd-869e9ade5126	107

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71335-1725-0	71335172500	42 TABLET in 1 BOTTLE (71335-1725-0)	42 tablet	2024-04-04	0000-00-00	No	No	Current
71335-1725-1	71335172501	30 TABLET in 1 BOTTLE (71335-1725-1)	30 tablet	2024-04-04	0000-00-00	No	No	Current
71335-1725-2	71335172502	60 TABLET in 1 BOTTLE (71335-1725-2)	60 tablet	2024-04-04	0000-00-00	No	No	Current
71335-1725-3	71335172503	90 TABLET in 1 BOTTLE (71335-1725-3)	90 tablet	2024-04-04	0000-00-00	No	No	Current
71335-1725-4	71335172504	120 TABLET in 1 BOTTLE (71335-1725-4)	120 tablet	2024-04-04	0000-00-00	No	No	Current
71335-1725-5	71335172505	14 TABLET in 1 BOTTLE, PLASTIC (71335-1725-5)	14 tablet	2024-04-04	0000-00-00	No	No	Current
71335-1725-6	71335172506	28 TABLET in 1 BOTTLE, PLASTIC (71335-1725-6)	28 tablet	2024-04-04	0000-00-00	No	No	Current
71335-1725-7	71335172507	6 TABLET in 1 BOTTLE, PLASTIC (71335-1725-7)	6 tablet	2020-10-23	0000-00-00	No	No	Current
71335-1725-8	71335172508	10 TABLET in 1 BOTTLE, PLASTIC (71335-1725-8)	10 tablet	2022-05-25	0000-00-00	No	No	Current
71335-1725-9	71335172509	21 TABLET in 1 BOTTLE, PLASTIC (71335-1725-9)	21 tablet	2024-04-04	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate	Bryant Ranch Prepack	2026-05-14	HUMAN PRESCRIPTION DRUG LABEL	107