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2770(E)

(Published in Part II, Section 3, Sub Section (ii) of the
Gazette of India Extraordinary, dated the 27th November, 2008)

Government of India
Ministry of Chemicals and Fertilizers
(National Pharmaceuticals Pricing Authority)

                                                                New Delhi, the 27th November, 2008

ORDER

S.O.2770(E)  – In exercise of the powers, conferred by sub-paragraphs (1) and (2) of paragraph 9 and paragraph 11 of the Drugs (Prices Control) Order, 1995, read with No. S.O. 637 (E) dated the 4th September, 1997 issued by the Government of India in the Ministry of Chemicals and Fertilizers, the National Pharmaceutical Pricing Authority, hereby fixes the prices as specified in column (5) of the table below as ceiling prices exclusive of excise duty and local tax, if any, and in column (6) of the table below as Equivalent MRP inclusive of excise duty and education cess, sales tax/VAT of each of the Scheduled formulations specified in the corresponding entry in column (2) of the said Table with the strength and pack size specified respectively in the corresponding entries in columns (3) and (4) thereof:

TABLE

Sl. No. Name of the Formulation Strength Pack Size Ceiling Price (Rs.) Equivalent MRP*(inclusive of all taxes)(Rs.)
(1) (2) (3) (4) (5) (6)

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Each bilayerd tablet contains

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1 Pseudoephedrine+
Desloratadine Tablets
Pseudoephedrine Sulphate – 120 mg
(as Extended Release)
Desloratadine – 2.5 mg
10’s Strip/Blister 7.68 8.45

--

Each sustained action tablets contains

--

2 Ephedrine+
Theophylline Tablets
Ephedrine Hydrochloride-48 mg
Theophylline (Hydrated)-198 mg
10’s Strip/Blister 5.46 6.01

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Each tablets contains

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3 Pseudoephedrine +
Cetrizine+
Nimesulide Tablets
Pseudoephedrine HCl – 60mg
Cetrizine Dihydrochloride-5mg
Nimesulide – 100 mg
10’s Strip/Blister 5.12 5.64

*Subject to actual payment of Government levies/taxes, as applicable.

NOTE :

(a)        The prices fixed are the maximum retail prices in column (6) (inclusive of excise duty and local taxes if any) for the specified pack and packs of similar strength, and companies cannot claim exemption on any ground therefrom, unless specifically permitted by the Government/NPPA through an order.

(b)        The companies / manufacturers may added taxes only if they have paid actually to the Government on the price mentioned in the column (5). If there is any variation in the MRP (inclusive of the taxes), the same may be intimated to the NPPA in the Form-V of DPCO, 1995.

(c)        Pro-rata pricing for packs of same composition but of different sizes will be applicable vide S.O. No. 83(E) dated 27.1.1998 for tablet and capsule packed in strip/blister.

(d)        For different packing material used or any special feature claimed, companies are required to approach NPPA for approval/fixation of specific prices.

(e)        The prices fixed/notified hereinabove under the provisions of DPCO, 1995 have to be mandatorily implemented by the manufacturing /marketing company notwithstanding its status of compliance of conditions for such formulation pack under the Drugs and Cosmetics Act, 1940.

(f)        The manufacturer and marketing company for the above said formulation shall be required to take the requisite prior approval from the competent Authority for any change in the composition of the above said formulation with written prior intimation to the National Pharmaceutical Pricing Authority.

(g)        The ceiling price arrived on the basis of above shall not exceed the MRP by multiplying the ceiling price by a factor of 1.1009 as per the existing rates of excise duty and VAT.

(h)        The MRP arrived as above shall be subject to payment of Government levies / taxes as applicable and necessary adjustment in the factor of 1.1009 shall necessarily be required to be made by the manufacturer/marketing company, whenever the existing rate of excise duty and/or VAT undergoes a change, subject to the condition that the excise duty and/or VAT so calculated shall in no case exceed the actual excise duty and/or VAT paid by the manufacturer/marketing company or as applicable as per the factor of 1.1009. The manufacturer/marketing company shall be specifically liable to ensure the compliance of this condition.

(i)        Any other formulation / composition not covered in the above table that has any one of the scheduled drugs in Column No. (3) as one of its ingredients, it shall be subject to the price ceiling at respective serial number of the table, as the case may be, unless the manufacturer has got hereafter specific price fixed by the NPPA for that formulation.

(j)        Consequent to the issue of ceiling price of the formulation pack(s) in this notification, the following price order(s) issued prior to this date of notification stand automatically withdrawn :

Sl.No. Price Order No. Date
. -- --

.and any other price order(s) issued earlier for the composition of the formulation pack for which ceiling price is notified in this notification.

PN/105/2008/F

F.No. 8(14)/2008/D.P./NPPA-Div.II

(RAJIV WADHAWAN)
Deputy Director
National Pharmaceutical Pricing Authority

Last Page Updated: 01-06-2019