FDA.reportPublic FDA data

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

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
IngredientStrength
BUPRENORPHINE HYDROCHLORIDE8 mg/1
NALOXONE HYDROCHLORIDE DIHYDRATE2 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii56W8MW3EN1, 5Q187997EE
Rxcui351267

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
68654759-f50b-79ef-24c5-544d94fe7d87Product name320251114
c955d208-c333-9bd7-be34-d7e12986d44eProduct name620250626
e5f98bfa-66d5-4c3a-b22d-9543d3bee304Product name120250204
caa6391e-3db3-c912-335f-61b5fc00aa12Product name920240110
08a295bb-88df-4ab0-a120-a75a789a74f1Product name120231013
65a3bc34-04ff-4cf1-aad9-c7d92a062f6dProduct name120231003
e951cdf3-f269-4d97-a7d5-c1c3d7283a7dProduct name320230313
ab841ac7-728a-4fc9-be0a-35b96cecbf39Product name420230306
100316cc-94a9-474e-97ad-9b5c6ddec605Product name520230125
f327b80c-8fa2-404b-838a-df3eec141cf2Product name120221212
d4aa2fcf-79c3-4b5f-a00e-1a8e26e00119Product name120220511
539bc5d3-546b-4af6-9c31-058ce6c459d3Product name220220210
b871fccd-1de6-4c7f-b9e5-045304641ee6Product name820220118
43b1efe2-1425-4b3e-b3a2-57d40f8478b9Product name120211026
31e16ab2-c562-4617-a3e8-ed285320e16eProduct name120180201
4c23a34c-e8fc-424c-8fa0-ee064ba6eaefProduct name120170706
a5920611-4285-f024-69b9-39ff338b81eaProduct name520170609
0b8c7273-1da3-495f-909a-7cf1e96d2361Product name120161212
3df867ed-9d48-45cf-bded-1394beaea0b1Product name320161206
973da5bf-b1f9-4de0-81ee-7ca066c98ca4Product name120160712
8a245632-e24f-4ccc-b671-995d89c96ebcProduct name120141203

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-1725-0Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate42 in 1 BOTTLETABLET42107
71335-1725-1Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate30 in 1 BOTTLETABLET30107
71335-1725-2Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate60 in 1 BOTTLETABLET60107
71335-1725-3Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate90 in 1 BOTTLETABLET90107
71335-1725-4Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate120 in 1 BOTTLETABLET120107
71335-1725-5Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate14 in 1 BOTTLE, PLASTICTABLET14107
71335-1725-6Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate28 in 1 BOTTLE, PLASTICTABLET28107
71335-1725-7Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate6 in 1 BOTTLE, PLASTICTABLET6107
71335-1725-8Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate10 in 1 BOTTLE, PLASTICTABLET10107
71335-1725-9Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate21 in 1 BOTTLE, PLASTICTABLET21107

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-1725-1EA - Each71335-1725a90e63b1-cac7-4672-af91-cbaa34eec6ee12022-10-06
71335-1725-2EA - Each71335-1725de161d5a-b02d-4a15-a385-4100a146dd5612022-10-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-1725BUPRENORPHINE HYDROCHLORIDE AND NALOXONE HYDROCHLORIDE DIHYDRATE TABLET [BRYANT RANCH PREPACK]106Current NDC, Legacy NDC, 10 package rows20240410_b9b5b1d5-482e-42ad-aabd-869e9ade5126.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
351267buprenorphine HCl 8 MG / naloxone HCl 2 MG Sublingual TabletPSNb9b5b1d5-482e-42ad-aabd-869e9ade5126107
351267buprenorphine 8 MG / naloxone 2 MG Sublingual TabletSCDb9b5b1d5-482e-42ad-aabd-869e9ade5126107
351267buprenorphine 8 MG (as buprenorphine HCl) / naloxone 2 MG (as naloxone HCl) Sublingual TabletSYb9b5b1d5-482e-42ad-aabd-869e9ade5126107

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1725-07133517250042 TABLET in 1 BOTTLE (71335-1725-0) 42 tablet2024-04-040000-00-00NoNoCurrent
71335-1725-17133517250130 TABLET in 1 BOTTLE (71335-1725-1) 30 tablet2024-04-040000-00-00NoNoCurrent
71335-1725-27133517250260 TABLET in 1 BOTTLE (71335-1725-2) 60 tablet2024-04-040000-00-00NoNoCurrent
71335-1725-37133517250390 TABLET in 1 BOTTLE (71335-1725-3) 90 tablet2024-04-040000-00-00NoNoCurrent
71335-1725-471335172504120 TABLET in 1 BOTTLE (71335-1725-4) 120 tablet2024-04-040000-00-00NoNoCurrent
71335-1725-57133517250514 TABLET in 1 BOTTLE, PLASTIC (71335-1725-5) 14 tablet2024-04-040000-00-00NoNoCurrent
71335-1725-67133517250628 TABLET in 1 BOTTLE, PLASTIC (71335-1725-6) 28 tablet2024-04-040000-00-00NoNoCurrent
71335-1725-7713351725076 TABLET in 1 BOTTLE, PLASTIC (71335-1725-7) 6 tablet2020-10-230000-00-00NoNoCurrent
71335-1725-87133517250810 TABLET in 1 BOTTLE, PLASTIC (71335-1725-8) 10 tablet2022-05-250000-00-00NoNoCurrent
71335-1725-97133517250921 TABLET in 1 BOTTLE, PLASTIC (71335-1725-9) 21 tablet2024-04-040000-00-00NoNoCurrent