Rifabutin

Product NDC
73141-020
11-digit product format
731410020
Labeler code
73141
Product ID
73141-020_52e7cb84-1fe6-54ce-e063-6294a90aa4b1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Rifabutin
Dosage form
CAPSULE
Route
ORAL
Labeler
A2A Integrated Pharmaceuticals
Application
ANDA212430
Marketing category
ANDA
Marketing start
2026-05-15
Substance
RIFABUTIN
Active strength
150 mg/1
Pharmacologic classes
Rifamycin Antimycobacterial [EPC], Rifamycins [CS]
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 43.

Orange Book products#

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

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A212430-001RIFABUTINRIFABUTIN150MGCAPSULE / ORALAB2026-03-19

Therapeutic equivalence codes#

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

Application-product, TE code table
Application-productTE code
A212430-001AB

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
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A212430-001RIFABUTIN150MGCAPSULE / ORALAB2026-03-1984e616aacf4f…
2026-08-18 06:07:402026-07A212430-001RIFABUTIN150MGCAPSULE / ORALAB2026-03-19caaa826d4ba7…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A212430-001RIFABUTIN150MGCAPSULE / ORALAB2026-03-19a50c72e98297…

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
CapturedEditionApplication-productTE codeOrderSource SHA-256
2026-09-14 22:38:342026-08A212430-001AB184e616aacf4f…
2026-08-18 06:07:402026-07A212430-001AB1caaa826d4ba7…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A212430-001AB1a50c72e98297…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Rifabutin
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
RIFABUTIN150 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1W306TDA6SInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
198200Internal RxNorm lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
10fb5949-5572-47bd-aaf0-018d9978cad8Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f33561b9-47cb-411c-a228-16c62e346cd4Product name120200415
48b3639b-9f6e-fb03-0720-42e7d1e139acProduct name120140508

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RifabutinRIFABUTINA2A Integrated Pharmaceuticals10fb5949-5572-47bd-aaf0-018d9978cad82026-05-15Warnings, Adverse reactionsExact identifier
application applno (ANDA): 212430
application number: ANDA212430
ndc (product): 73141-020
RifabutinRIFABUTINi3 Pharmaceuticals, LLCfd6062e2-17c8-48f4-a1fe-69ebe410f5832026-02-20Warnings, Adverse reactionsExact identifier
application applno (ANDA): 212430
application number: ANDA212430

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
73141-020-0473141002004100 CAPSULE in 1 BOTTLE (73141-020-04) 100 capsule2026-05-15NoNoCurrent