NDC 55648-101-08 - Bupropion Hydrochloride (SR)

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 55648-101
Requested NDC: 55648-101-08
Package NDCs from labels: 55648-101-01, 55648-101-02, 55648-101-03, 55648-101-07, 55648-101-08, 55648-101-05
Manufacturer: Wockhardt Limited
Effective date: 2012-11-06
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Bupropion Hydrochloride (SR) - Wockhardt Limited	Wockhardt Limited	2012-11-06	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Related label table
NDC	Related label
55648-101-01	PRESCRIBING INFORMATION Bupropion Hydrochloride Extended-Release Tablets, USP (SR)
55648-101-02	PRESCRIBING INFORMATION Bupropion Hydrochloride Extended-Release Tablets, USP (SR)
55648-101-03	PRESCRIBING INFORMATION Bupropion Hydrochloride Extended-Release Tablets, USP (SR)
55648-101-05	PRESCRIBING INFORMATION Bupropion Hydrochloride Extended-Release Tablets, USP (SR)
55648-101-07	PRESCRIBING INFORMATION Bupropion Hydrochloride Extended-Release Tablets, USP (SR)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
55648-101-01	Bupropion Hydrochloride(SR)	30 in 1 BOTTLE	TABLET, FILM COATED, EXTENDED RE	30	2
55648-101-02	Bupropion Hydrochloride(SR)	60 in 1 BOTTLE	TABLET, FILM COATED, EXTENDED RE	60	2
55648-101-03	Bupropion Hydrochloride(SR)	100 in 1 BOTTLE	TABLET, FILM COATED, EXTENDED RE	100	2
55648-101-05	Bupropion Hydrochloride(SR)	10 in 1 CARTON	TABLET, FILM COATED, EXTENDED RE	10	2
55648-101-07	Bupropion Hydrochloride(SR)	500 in 1 BOTTLE	TABLET, FILM COATED, EXTENDED RE	500	2
55648-101-08	Bupropion Hydrochloride(SR)	10 in 1 BLISTER PACK	TABLET, FILM COATED, EXTENDED RE	10	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55648-101	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2	Legacy NDC, 6 package rows	20121107_1a2a5385-ec04-448f-8bdb-d1cc3eb5f1c0.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
BUPROPION HYDROCHLORIDE	ACTIVE INGREDIENT	ZG7E5POY8O	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
BUPROPION	ACTIVE MOIETY	01ZG3TPX31	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
AMMONIUM CHLORIDE	INACTIVE INGREDIENT	01Q9PC255D	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
FD&C BLUE NO. 1	INACTIVE INGREDIENT	H3R47K3TBD	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
GLYCERYL DIBEHENATE	INACTIVE INGREDIENT	R8WTH25YS2	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
HYDROXYPROPYL CELLULOSE	INACTIVE INGREDIENT	RFW2ET671P	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
STEARIC ACID	INACTIVE INGREDIENT	4ELV7Z65AP	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	BUPROPION HYDROCHLORIDE (SR) (BUPROPION HYDROCHLORIDE) TABLET, FILM COATED, EXTENDED RELEASE [WOCKHARDT LIMITED]	2

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 96 of 141 · 2,819 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 CARAMEL	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29a82ba9-c0f8-0edf-e063-6294a90a50b4	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 SABLE	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29a8812b-70ff-e8aa-e063-6294a90a09f8	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
CLE CCC Neutral Deep	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, AVOBENZONE	KW ABSC, INC.	3a548deb-3670-4c5b-a139-796701801fed	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
CLE CCC Olive Medium Deep	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	be4434c0-cbdd-46cb-8015-4c7859e80d4a	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
CLE CCC Golden Medium	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	de50e956-a014-4147-922b-63c95fa6f86b	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
CLE CCC Neutral Light	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	44cbb226-83ed-401b-baf8-ca8e4740dbef	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
CLE CCC Neutral Medium Light	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	615f5e39-695d-41d4-af59-e0d3b76789bb	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
CLE CCC Warm Deep	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, AVOBENZONE	KW ABSC, INC.	6ab3e360-8104-4439-93fb-e11bc4a77558	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
CLE CCC Neutral Medium	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	a297ff64-678c-4936-8384-022606a2f33c	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
CLE CCC Neutral Fair	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	aa8176c6-f1c9-43dd-96e0-f7d6ed30a1a2	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
CLE CCC Cool Medium Deep	TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE	KW ABSC, INC.	2e0365f9-d3c6-4404-90ac-772a829b3ade	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18- D2 NUTMEG	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29abae8f-53db-b592-e063-6294a90adabb	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 MOCHA	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29aba80c-55b7-b8d9-e063-6294a90a5cc1	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 COCOA	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29abe97b-e9b3-6e27-e063-6294a90ae3ed	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 DEEP GOLDEN	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29abdf3c-fb54-a5e3-e063-6394a90af450	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
Bupropion Hydrochloride (XL)	BUPROPION HYDROCHLORIDE	Quality Care Products, LLC	57a9f4d3-0c41-4978-b81e-cf3059bc8c42	2024-12-19	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: ZG7E5POY8O
Trace Mineral Cord	ARGENTUM METALLICUM, AURUM METALLICUM, BORON CITRATE, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, CHROMIUM SULPHURICUM, COBALT GLUCONATE, CUPRUM SULPHURICUM, FERRUM PHOSPHORICUM, GERMANIUM SESQUIOXIDE, IODIUM, KALI BROMATUM, KALI MURIATICUM, KALI PHOSPHORICUM, KALI SULPHURICUM, LITHIUM CARBONICUM, MAGNESIA PHOSPHORICA, MANGANUM MURIATICUM, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, SELENIUM METALLICUM, SILICEA, SODIUM MOLYBDATE, STRONTIUM CARBONICUM, VANADIUM METALLICUM,	Energique, Inc.	902dd68d-5ce1-481e-8938-6487dcc68dfc	2024-12-19	Warnings	Exact identifier unii: ETJ7Z6XBU4
CeraVe Developed with Dermatologists Hydrating Mineral Sunscreen Broad Spectrum SPF 30 Face Sheer Tint Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	L'Oreal USA Products, Inc.	f2e34230-7bfb-455f-8b33-6bff96fd9f0a	2024-12-19	Warnings	Exact identifier unii: 15FIX9V2JP
Light Illusion Luminous Makeup Nude-Skin Feel SPF18 SHELL	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	COSMAX USA, INC	29868d60-b900-e0ad-e063-6294a90af87a	2024-12-18	Warnings	Exact identifier unii: 15FIX9V2JP
Belasol Suncream Non Tinted Moisturizing Sunscreen SPF 50 Jasmine	TITANIUM DIOXIDE, ZINC OXIDE	EK Clothing LLC dba Belasol	e999d752-6c00-459e-b6c3-d264c330597d	2024-12-18	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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