SUPREME COURT OF INDIA
Commissioner of Central Excise, Mumbai
Vs.
Johnson and Johnson Limited
C.A.Nos.8277-8280
(Mrs.Ruma Pal and P. P. Naolekar JJ.)
22.09.2005
JUDGMENT
Ruma Pal, J.
1. The respondents import medicines which are classifiable under Chapter
Heading 3003.10 of the Central Excise Tariff Act, 1985(hereinafter
referred to as 'the Act'). We are concerned with the import of two particular
medicines, namely, Eprex and Topamac. The question is whether these two
medicaments were manufactured for the purposes of attracting duty under the
Act.
2. Note 5 Chapter 30 has extended the meaning of 'manufacturers' and reads as
follows:
"In relation to products of Heading No. 30.03, conversion of powder into
tablets or capsules, labelling or relabelling of containers intended for
consumers and repacking from bulk packs to retail packs or the adoption of any
other treatment to render the product marketable to the consumer, shall amount
to 'manufacture'."
3. According to the Customs Excise and Service Tax Tribunal merely labelling or
relabelling of the containers intended for consumers would not do, The products
would have to be repacked from bulk packs to retail packs so as to render the
Product marketable to the consumer for the activity to be termed as
'manufacture'.
4. The learned Additional Solicitor appearing on behalf of the appellant has
impugned the decision of the Tribunal and has submitted that admittedly in this
case there was labelling after the medicaments were imported. As far as
repacking was concerned, it is submitted that the goods were imported in
pallets with one big box containing two smaller boxes. The smaller boxes
contained as sorted medicines of different potencies. These assorted medicines
were in smaller units. The Eprex units contained syringes with six vials. These
units were removed from the boxes, repacked in thermocole boxes of different
sizes which were again put into cardboard boxes which were then marketed.
5. Similarly, as far as the Topamac was concerned, each unit consisted of ten
tablets which were also put into cardboard boxes and marketed after the units
were labelled. It is stated that the cardboard boxes in both the cases were in
turn labelled containing, inter alia, the name of the medicine, the name of
manufacture, the quantity, batch number, manufacturing date, expiry date and
name of the marketing agency. Our attention has been drawn to the statement of
the parties given under Section 14 of the Central Excise Act, 1944, by
the agent of the respondent. The statement confirmed, inter alia, that there
was repacking and labelling of the medicaments before sale to the dealer and
stock transfer to other depots.
6. What has been overlooked by the appellant is that merely packing for being
marketed would not do. The repacking would have to be from bulk packs to
"retail packs" so as to render the product marketable directly to the
consumer. There is no evidence relied upon by the appellants to the effect that
the cardboard boxes in which the units were placed or the thermocole containers
were "retail packs".
7. In that view of the matter, the appeals are dismissed but without any order
as to costs.
C.A. Nos. 8728-8732/2003:
8. The respondents import items classifiable under Chapter 18 and Chapter 19 of
the Central Excise Tariff Act, 1985 (hereinafter referred to
as 'the Act'). The issue is whether Note 3 to Chapter 18 and Note 3 to Chapter
19 which extend the meaning of manufacture by legal fiction to the labelling or
relabelling of containers and repacking from bulk to retail packs would apply.
For the reasons stated by us in the order passed in C.A. Nos. 8277-8280/2003
these appeals are also dismissed.
9. In these appeals there is an additional fact that the Commissioner of
Central Excise had found as a fact that the products are imported as ready for
sale to consumers in retail packs. These retail packs were then taken to the
appellant's warehouses where stickers were affixed to them containing
information like names and addresses of the importers, maximum retail price,
net weight etc. In these cases the appellants therefore, admittedly merely
imported ready to market retail packs. There is no evidence of the appellants'
themselves indulging in any further activity which required the packing or
repacking of bulk packing into retail packs within the extended meaning of
'manufacture' as contained in Chapter Note 3 in Chapters 18 and 19 of the Act.
10. The appeals are dismissed but without any order as to costs.