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1337(E)

(Published in Part II, Section 3, Sub Section (ii) of the
Gazette of India Extraordinary, dated the 5th June, 2008)

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

                                                                New Delhi, the 5th June, 2008

ORDER

S.O.1337(E)  – In exercise of the powers, conferred by sub-paragraph (1)/(2)/(4) of paragraph 8 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/revises the prices as specified in column (5) of the table hereto annexed as the retail price/revised retail price, exclusive of excise duty, Sales Taxes/VAT and local taxes, if any, and in column (6) as equivalent MRP inclusive of excise duty, education cess, Sales Tax/VAT in relation to each of the formulation specified in the corresponding entry in column (2) of the said table with the pack size specified in the corresponding entries in column (3) thereof; manufactured/imported by M/s. Pfizer Products India Pvt. Ltd.

TABLE

Sl. No. Name of the Formulation Pack Size Existing Retail Price (Rs.) Retail Price without Excise Duty Sales Tax /VAT and Local Tax, if any (Rs.) Equivalent MRP*(inclusive of all taxes)(Rs.)
(1) (2) (3) (4) (5) (6)
1 Depomedrol 40mg
Each ml contains
Methyl Prednisolone Acetate – 40mg
Batch No. R00204 Qty. 116524
1ml vial 48.67 49.65 51.64
2 Depomedrol 80mg
Each ml contains
Methyl Prednisolone Acetate – 80mg
Batch No. R01131 Qty. 157012
Batch No. R00210 Qty. 100503
2ml vial 71.89 72.98 75.90
3 Solu Medrol 125mg AOV
Each Vial contains
Methyl Prednisolone Sodium Succinate – 125mg
Batch No. R00062 Qty. 47583
2ml vial 227.75 231.75 241.02
4 Solu Medrol AOV 500mg
Each Vial contains
Methyl Prednisolone Sodium Succinate – 500mg
Batch No. OAKKO Qty. 23197
Batch No. OAMF6 Qty. 23236
4ml vial 555.54 560.52 582.94
5 Solu Medrol AOV 1000mg
Each Vial contains
Methyl Prednisolone Sodium Succinate – 1000mg
Batch No. OAMXJ Qty. 34780
8ml vial 895.51 910.55 946.97
6 Medrol 4mg tablets
Each tablet contains
Methyl Prednisolone – 4mg
Batch No. G902C Qty. 11308
Batch No. G604A Qty. 32568
Batch No. G904A & G905A Qty. 17680
Batch No. G904A & G902C Qty. 34526
Batch No. G603B Qty. 11048
10×10’s Tablet 289.95 294.71 306.50
7 Medrol 16mg tablets
Each tablet contains
Methyl Prednisolone – 16mg
Batch No. G933A Qty. 48096
14’s Tablet 127.62 129.64 134.83

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

NOTE :

(a)        The prices fixed are the maximum retail prices in column no. (6) (inclusive of excise duty, sales tax/VAT 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)        For different packing material used or any special feature claimed, companies are required to approach NPPA for approval/fixation of specific prices.

(d)        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.

(e)        These prices/revised prices shall be made effective within 15 days of receipt of this order as required under sub para 14(1) of DPCO, 1995. The necessary price-list should also be issued as required under sub-paragraph (3) of paragraph 14 of the Drugs (Prices Control) Order, 1995.

(f)        These 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.

PN/101/2008/F

F.No. 8(11)/2008/D.P./NPPA-Div.II

(RAJIV WADHAWAN)
Deputy Director
National Pharmaceutical Pricing Authority

Last Page Updated: 03-06-2019