Divalproex Sodium

Product NDC: 29300-140
11-digit product format: 293000140
Labeler code: 29300
Product ID: 29300-140_8e888ed9-2d55-4e95-ba7b-8b437481c947
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Divalproex Sodium
Dosage form: TABLET, DELAYED RELEASE
Route: ORAL
Labeler: Unichem Pharmaceuticals (USA), Inc.
Application: ANDA079163
Marketing category: ANDA
Marketing start: 2011-10-01
Substance: DIVALPROEX SODIUM
Active strength: 500 mg/1
Pharmacologic classes: Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Additional Listing Data#

Finished product: Yes
Brand name base: Divalproex Sodium
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
DIVALPROEX SODIUM	500 mg/1

Harmonized Identifiers#

Field, Values table
Field	Values
Unii	644VL95AO6
Rxcui	1099625, 1099678, 1099870

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
b10a892b-b985-4cbc-9547-9ac4b72b784f	Product name	2	20250818
7a3a03f1-382a-f9ec-0741-ff24dcbfed69	Product name	7	20250624
fb7ab793-2c12-4079-b100-a64f73bef25a	Product name	4	20240712
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829
b0cbf770-6cc3-4aa4-9158-755110c2b9f7	Product name	2	20230717
dc7c5daa-021f-40dd-b00d-63982cb2067a	Product name	1	20230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	5	20200925
57fc3d01-4737-4091-9728-9e8a4c9e708d	Product name	1	20200121
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89f	Product name	2	20160823
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
5d67ecc7-47c7-ec5e-e9eb-71bf00250645	Product name	1	20140508
97fce1a8-50c4-f088-0e31-64d82b6e9081	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
29300-140-01	Divalproex Sodium	100 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	100	26
29300-140-05	Divalproex Sodium	500 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	500	26
29300-140-10	Divalproex Sodium	1000 in 1 BOTTLE, PLASTIC	TABLET, DELAYED RELEASE	1000	26

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
29300-140-01	EA - Each	29300-140	d3dcc4d6-fe79-4e90-966a-6794bc794508	1	2012-07-24
29300-140-05	EA - Each	29300-140	eafb9e8d-fd48-4793-ba54-cdec605dbdfb	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
DIVALPROEX SODIUM	ACTIVE INGREDIENT	644VL95AO6	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
VALPROIC ACID	ACTIVE MOIETY	614OI1Z5WI	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
BUTYL ALCOHOL	INACTIVE INGREDIENT	8PJ61P6TS3	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
FERROSOFERRIC OXIDE	INACTIVE INGREDIENT	XM0M87F357	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
HYPROMELLOSE 2910 (6 MPA.S)	INACTIVE INGREDIENT	0WZ8WG20P6	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A	INACTIVE INGREDIENT	NX76LV5T8J	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
POLYETHYLENE GLYCOL 3000	INACTIVE INGREDIENT	SA1B764746	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
POVIDONE K29/32	INACTIVE INGREDIENT	390RMW2PEQ	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
SHELLAC	INACTIVE INGREDIENT	46N107B71O	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
SODIUM BICARBONATE	INACTIVE INGREDIENT	8MDF5V39QO	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
TRIACETIN	INACTIVE INGREDIENT	XHX3C3X673	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
VANILLIN	INACTIVE INGREDIENT	CHI530446X	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [BRYANT RANCH PREPACK]	1005
DIVALPROEX SODIUM	ACTIVE INGREDIENT	644VL95AO6	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
VALPROIC ACID	ACTIVE MOIETY	614OI1Z5WI	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
BUTYL ALCOHOL	INACTIVE INGREDIENT	8PJ61P6TS3	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
D&C RED NO. 30	INACTIVE INGREDIENT	2S42T2808B	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
FERROSOFERRIC OXIDE	INACTIVE INGREDIENT	XM0M87F357	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
HYPROMELLOSE 2910 (6 MPA.S)	INACTIVE INGREDIENT	0WZ8WG20P6	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A	INACTIVE INGREDIENT	NX76LV5T8J	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
POLYETHYLENE GLYCOL 3000	INACTIVE INGREDIENT	SA1B764746	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
POVIDONE K29/32	INACTIVE INGREDIENT	390RMW2PEQ	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
SHELLAC	INACTIVE INGREDIENT	46N107B71O	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
SODIUM BICARBONATE	INACTIVE INGREDIENT	8MDF5V39QO	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
STARCH, PREGELATINIZED CORN	INACTIVE INGREDIENT	O8232NY3SJ	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
TRIACETIN	INACTIVE INGREDIENT	XHX3C3X673	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
VANILLIN	INACTIVE INGREDIENT	CHI530446X	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	10
DIVALPROEX SODIUM	ACTIVE INGREDIENT	644VL95AO6	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
DIVALPROEX SODIUM	ACTIVE INGREDIENT	644VL95AO6	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
VALPROIC ACID	ACTIVE MOIETY	614OI1Z5WI	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
VALPROIC ACID	ACTIVE MOIETY	614OI1Z5WI	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
BUTYL ALCOHOL	INACTIVE INGREDIENT	8PJ61P6TS3	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
BUTYL ALCOHOL	INACTIVE INGREDIENT	8PJ61P6TS3	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
COLLOIDAL SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
FD&C RED NO. 40	INACTIVE INGREDIENT	WZB9127XOA	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
FERROSOFERRIC OXIDE	INACTIVE INGREDIENT	XM0M87F357	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
FERROSOFERRIC OXIDE	INACTIVE INGREDIENT	XM0M87F357	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
HYPROMELLOSE 2910 (6 MPA.S)	INACTIVE INGREDIENT	0WZ8WG20P6	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
HYPROMELLOSE 2910 (6 MPA.S)	INACTIVE INGREDIENT	0WZ8WG20P6	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
ISOPROPYL ALCOHOL	INACTIVE INGREDIENT	ND2M416302	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A	INACTIVE INGREDIENT	NX76LV5T8J	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A	INACTIVE INGREDIENT	NX76LV5T8J	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
POLYETHYLENE GLYCOL 3000	INACTIVE INGREDIENT	SA1B764746	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
POLYETHYLENE GLYCOL 3000	INACTIVE INGREDIENT	SA1B764746	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
SHELLAC	INACTIVE INGREDIENT	46N107B71O	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
SHELLAC	INACTIVE INGREDIENT	46N107B71O	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
SODIUM BICARBONATE	INACTIVE INGREDIENT	8MDF5V39QO	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
SODIUM BICARBONATE	INACTIVE INGREDIENT	8MDF5V39QO	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
STARCH, CORN	INACTIVE INGREDIENT	O8232NY3SJ	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
STARCH, PREGELATINIZED CORN	INACTIVE INGREDIENT	O8232NY3SJ	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
TRIACETIN	INACTIVE INGREDIENT	XHX3C3X673	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
TRIACETIN	INACTIVE INGREDIENT	XHX3C3X673	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1
VANILLIN	INACTIVE INGREDIENT	CHI530446X	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [DIRECTRX]	1
VANILLIN	INACTIVE INGREDIENT	CHI530446X	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [STATE OF FLORIDA DOH CENTRAL PHARMACY]	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
29300-140	DIVALPROEX SODIUM TABLET, DELAYED RELEASE [UNICHEM PHARMACEUTICALS (USA), INC.]	23	Current NDC, Legacy NDC, 3 package rows	20250223_1ec1a441-218a-4c80-a0cb-69bcc327f472.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
644VL95AO6	DIVALPROEX SODIUM	76584-70-8	DIVALPROEX SODIUM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	PSN	c8d9cd69-ceca-3057-9d1c-12c44b19f767	1014
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	SCD	c8d9cd69-ceca-3057-9d1c-12c44b19f767	1014
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	PSN	79e6dc26-a38b-4642-a216-1fa1213b919a	104
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	SCD	79e6dc26-a38b-4642-a216-1fa1213b919a	104
1099625	divalproex sodium 125 MG Delayed Release Oral Tablet	PSN	1ec1a441-218a-4c80-a0cb-69bcc327f472	26
1099678	divalproex sodium 250 MG Delayed Release Oral Tablet	PSN	1ec1a441-218a-4c80-a0cb-69bcc327f472	26
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	PSN	1ec1a441-218a-4c80-a0cb-69bcc327f472	26
1099625	divalproex sodium 125 MG Delayed Release Oral Tablet	SCD	1ec1a441-218a-4c80-a0cb-69bcc327f472	26
1099678	divalproex sodium 250 MG Delayed Release Oral Tablet	SCD	1ec1a441-218a-4c80-a0cb-69bcc327f472	26
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	SCD	1ec1a441-218a-4c80-a0cb-69bcc327f472	26
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	PSN	beba3da1-e80d-45b4-9bd6-3ed85c9482f3	10
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	SCD	beba3da1-e80d-45b4-9bd6-3ed85c9482f3	10
1099678	divalproex sodium 250 MG Delayed Release Oral Tablet	PSN	abac11e6-7ce1-491c-9ac3-61f3df54c4a4	5
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	PSN	abac11e6-7ce1-491c-9ac3-61f3df54c4a4	5
1099678	divalproex sodium 250 MG Delayed Release Oral Tablet	SCD	abac11e6-7ce1-491c-9ac3-61f3df54c4a4	5
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	SCD	abac11e6-7ce1-491c-9ac3-61f3df54c4a4	5
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	PSN	ce12c7b1-caa9-4224-bb5f-3e20e0281d66	4
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	SCD	ce12c7b1-caa9-4224-bb5f-3e20e0281d66	4
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	PSN	485123a6-15c2-48f8-9ec5-3287f3effb3a	2
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	SCD	485123a6-15c2-48f8-9ec5-3287f3effb3a	2
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	PSN	2b818ac6-9e6d-4b8f-bb8c-e79c7bd03360	1
1099870	divalproex sodium 500 MG Delayed Release Oral Tablet	SCD	2b818ac6-9e6d-4b8f-bb8c-e79c7bd03360	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
29300-140-01	29300014001	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-01)	2011-10-01	0000-00-00	No	No	Current
29300-140-05	29300014005	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-05)	2011-10-01	0000-00-00	No	No	Current
29300-140-10	29300014010	1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-10)	2011-10-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Divalproex Sodium	REMEDYREPACK INC.	2026-05-22	HUMAN PRESCRIPTION DRUG LABEL	10
Divalproex Sodium	Unichem Pharmaceuticals (USA), Inc. \| Unichem Laboratories Limited, India \| Unichem Laboratories Limited	2026-04-20	HUMAN PRESCRIPTION DRUG LABEL	26
DIVALPROEX SODIUM	DirectRx	2026-03-17	HUMAN PRESCRIPTION DRUG LABEL	4
Divalproex Sodium	Bryant Ranch Prepack	2025-10-21	HUMAN PRESCRIPTION DRUG LABEL	104
Divalproex Sodium	Bryant Ranch Prepack	2025-03-25	HUMAN PRESCRIPTION DRUG LABEL	1014
Divalproex Sodium	Proficient Rx LP	2022-08-01	HUMAN PRESCRIPTION DRUG LABEL	5
Divalproex Sodium	Carilion Materials Management	2015-08-11	HUMAN PRESCRIPTION DRUG LABEL	2
Divalproex Sodium	State of Florida DOH Central Pharmacy	2015-01-03	HUMAN PRESCRIPTION DRUG LABEL	1

Divalproex Sodium

Additional Listing Data#

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Harmonized Identifiers#

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DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

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