(Published in Part II, Section 3, Sub Section (ii) of the Gazette of India
Extraordinary, dated the 20th july, 2000)
Government of India
Ministry of Chemicals and Fertilizers
National Pharmaceuticals Pricing Authority
New Delhi, the 20th July, 2000
S.O. 681(E) – In exercise of the powers, conferred by sub-paragraph (1) and (2) of paragraph 9 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, 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 | Price (Rs.) |
---|---|---|---|---|
(1) | (2) | (3) | (4) | (5) |
-- |
-- |
Each tab. contains | -- |
-- |
“1. | Erythromycin Estolate Tab | Erythromycin Estolateeq. to Erythromycin base125mg |
10’s Strip/Blister | 15.02 |
2. | Erythromycin Estolate Tab | Erythromycin Estolate eq. to Erythromycin base 250 mg |
10’s Strip/Blister | 29.04 |
3. | Erythromycin Estolate Tab | Erythromycin Estolate eq. to Erythromycin base 500 mg |
10’s Strip/Blister |
57.32 |
-- |
-- |
Each 5 ml contains | -- |
-- |
4. | Erythromycin Estolate Syrup/Suspension |
Erythromycin Estolate eq. to Erythromycin base 125 mg |
60 ml Bottle with M. Cup |
23.44 |
Note :
1. The above ceiling prices mentioned in the column no. 5 are applicable to all manufacturers/formulators who are using either imported Erythromycin Estolate or Erythromycin Estolate manufactured from imported TIOC (Erythromycin Thiocynate).
2 (i) The ceiling prices of Erythromycin Estolate formulation notified vide S.O. No. 195(E) dated 11th March, 1998 shall be applicable to only those formulators/manufacturers who are using Erythromycin Estolate manufactured from TIOC produced from basic stage of fermentation in the country.
2 (ii) Such manufacturers/formulators are required to submit quarterly production return by 10th of January, April, July and October of its preceeding quarter to Govt./NPPA giving details of in-house production of bulk drug, purchase of bulk drug, showing separately Erythromycin Estolate made out of indigenous and imported TIOC and consumption thereof in production of formulations as per proforma which has been prescribed.
PN/38/2000/F
F. No. 8(27)/2000/D.P./NPPA-Div.II
(L. M. Kaushal)
Deputy Director
National Pharmaceutical
Pricing Authority
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