MedPath
FDA Approval

Lamivudine Zidovudine

June 22, 2016

HUMAN PRESCRIPTION DRUG LABEL

Lamivudine(150 mg in 1 1)
Zidovudine(300 mg in 1 1)

Manufacturing Establishments (1)

Direct Rx

Direct Rx

079254320

Products (1)

Lamivudine Zidovudine

61919-061

ANDA202418

ANDA (C73584)

ORAL

June 22, 2016

SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4Class: IACT
HYPROMELLOSE 2910 (6 MPA.S)Inactive
Code: 0WZ8WG20P6Class: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30Class: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61UClass: IACT
POLYETHYLENE GLYCOL 400Inactive
Code: B697894SGQClass: IACT
POLYSORBATE 80Inactive
Code: 6OZP39ZG8HClass: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2Class: IACT
TITANIUM DIOXIDEInactive
Code: 15FIX9V2JPClass: IACT
Code: 2T8Q726O95Class: ACTIBQuantity: 150 mg in 1 1
Code: 4B9XT59T7SClass: ACTIBQuantity: 300 mg in 1 1
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