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Approved Drug Products of Merck Group listed in the FDA Orange Book. Original Data : FDA Website

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01 AVELUMAB (2)

02 CETRORELIX ACETATE (2)

03 CHORIOGONADOTROPIN ALFA (2)

04 CLADRIBINE (1)

05 CLOMIPHENE CITRATE (1)

06 FOLLITROPIN ALFA/BETA (12)

07 INTERFERON BETA-1A (2)

08 LEVOTHYROXINE SODIUM (11)

09 MENOTROPINS (FSH;LH) (2)

10 METFORMIN HYDROCHLORIDE (7)

11 MITOXANTRONE HYDROCHLORIDE (4)

12 SERMORELIN ACETATE (3)

13 SOMATROPIN (9)

14 SOMATROPIN RECOMBINANT (4)

15 TEPOTINIB HYDROCHLORIDE (1)

16 UROFOLLITROPIN (4)

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01 INJECTABLE; INJECTION (1)

02 INJECTABLE;INJECTION (22)

03 INJECTABLE;INTRAMUSCULAR (2)

04 INJECTABLE;INTRAVENOUS (1)

05 INJECTABLE;SUBCUTANEOUS (16)

06 POWDER;SUBCUTANEOUS (2)

07 SYRINGE (2)

08 TABLET, EXTENDED RELEASE;ORAL (2)

09 TABLET;ORAL (19)

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01 0.025MG (1)

02 0.05MG (1)

03 0.075MG (1)

04 0.088MG (1)

05 0.112MG (1)

06 0.125MG (1)

07 0.15MG (1)

08 0.175MG (1)

09 0.1MG (1)

10 0.25MG/VIAL (1)

11 0.2MG (1)

12 0.3MG (1)

13 1,050 IU/VIAL (1)

14 10MG (1)

15 150 IU/0.25ML (1)

16 150 IU/AMP (2)

17 150 IU/AMP;150 IU/AMP (1)

18 150 IU/VIAL (2)

19 1GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

20 20MG/ML (2)

21 22UG/0.5ML (1)

22 300 IU/0.5ML (1)

23 37.5 IU/VIAL (2)

24 44UG/0.5ML (1)

25 450 IU/0.75ML (1)

26 450 IU/VIAL (1)

27 4MG/VIAL (3)

28 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (2)

29 50MG (1)

30 5MG/VIAL (3)

31 625MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

32 6MG/0.5ML (6MG/0.5ML) (1)

33 6MG/VIAL (3)

34 75 IU/AMP (2)

35 75 IU/AMP;75 IU/AMP (1)

36 75 IU/VIAL (2)

37 750MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (2)

38 8.8MG/VIAL (3)

39 850MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

40 900 IU/1.5ML (1)

41 EQ 0.05MG BASE/AMP **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

42 EQ 0.25MG /0.5ML (1)

43 EQ 0.25MG BASE/VIAL (1)

44 EQ 0.5MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

45 EQ 1MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

46 EQ 20MG BASE/10ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

47 EQ 225MG BASE (1)

48 EQ 25MG BASE/12.5ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

49 EQ 2MG BASE/ML (1)

50 EQ 30MG BASE/15ML (EQ 2MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** (1)

51 EQ 3MG BASE/VIAL (1)

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01 DISCN (26)

02 RX (3)

03 Blank (38)

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INJECTABLE; INJECT...
20MG/ML
761049
BAVENCIO
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INJECTABLE; INTRAV...
20MG/ML
761078
BAVENCIO
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POWDER; SUBCUTANEO...
EQ 0.25MG BASE/VIA...
2000-08-11
21197
CETROTIDE
RX
Yes
AP
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POWDER; SUBCUTANEO...
EQ 3MG BASE/VIAL
2000-08-11
21197
CETROTIDE
DISCN
Yes
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INJECTABLE; INJECT...
0.25MG/VIAL
21149
OVIDREL
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INJECTABLE; SUBCUT...
EQ 0.25MG /0.5ML
21149
OVIDREL
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TABLET; ORAL
10MG
2019-03-29
22561
MAVENCLAD
RX
Yes
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TABLET; ORAL
50MG
1982-03-22
18361
SEROPHENE
DISCN
No
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INJECTABLE; SUBCUT...
75 IU/VIAL
21765
GONAL-F RFF
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INJECTABLE; SUBCUT...
150 IU/VIAL
21765
GONAL-F
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